|
NM_000501.4:c.1697C>T
(ELN)
MANE Select
|
NP_000492.2:p.Ala566Val
|
|
ENST00000252034.12:c.1697C>T
(ELN)
MANE Select
|
ENSP00000252034.7:p.Ala566Val
|
|
NM_000501.3:c.1697C>T
(ELN)
|
NP_000492.2:p.Ala566Val
|
|
NM_001081752.2:c.1610C>T
(ELN)
|
NP_001075221.1:p.Ala537Val
|
|
NM_001081752.3:c.1610C>T
(ELN)
|
NP_001075221.1:p.Ala537Val
|
|
NM_001081753.2:c.1655C>T
(ELN)
|
NP_001075222.1:p.Ala552Val
|
|
NM_001081753.3:c.1655C>T
(ELN)
|
NP_001075222.1:p.Ala552Val
|
|
NM_001081754.2:c.1712C>T
(ELN)
|
NP_001075223.1:p.Ala571Val
|
|
NM_001081754.3:c.1712C>T
(ELN)
|
NP_001075223.1:p.Ala571Val
|
|
NM_001081755.2:c.1640C>T
(ELN)
|
NP_001075224.1:p.Ala547Val
|
|
NM_001081755.3:c.1640C>T
(ELN)
|
NP_001075224.1:p.Ala547Val
|
|
NM_001278912.1:c.1697C>T
(ELN)
|
NP_001265841.1:p.Ala566Val
|
|
NM_001278912.2:c.1697C>T
(ELN)
|
NP_001265841.1:p.Ala566Val
|
|
NM_001278913.1:c.1454C>T
(ELN)
|
NP_001265842.1:p.Ala485Val
|
|
NM_001278913.2:c.1454C>T
(ELN)
|
NP_001265842.1:p.Ala485Val
|
|
NM_001278914.1:c.1625C>T
(ELN)
|
NP_001265843.1:p.Ala542Val
|
|
NM_001278914.2:c.1625C>T
(ELN)
|
NP_001265843.1:p.Ala542Val
|
|
NM_001278915.1:c.1715C>T
(ELN)
|
NP_001265844.1:p.Ala572Val
|
|
NM_001278915.2:c.1715C>T
(ELN)
|
NP_001265844.1:p.Ala572Val
|
|
NM_001278916.1:c.1553C>T
(ELN)
|
NP_001265845.1:p.Ala518Val
|
|
NM_001278916.2:c.1553C>T
(ELN)
|
NP_001265845.1:p.Ala518Val
|
|
NM_001278917.1:c.1667C>T
(ELN)
|
NP_001265846.1:p.Ala556Val
|
|
NM_001278917.2:c.1667C>T
(ELN)
|
NP_001265846.1:p.Ala556Val
|
|
NM_001278918.1:c.1430C>T
(ELN)
|
NP_001265847.1:p.Ala477Val
|
|
NM_001278918.2:c.1430C>T
(ELN)
|
NP_001265847.1:p.Ala477Val
|
|
NM_001278939.1:c.1784C>T
(ELN)
|
NP_001265868.1:p.Ala595Val
|
|
NM_001278939.2:c.1784C>T
(ELN)
|
NP_001265868.1:p.Ala595Val
|
|
ENST00000252034.11:c.1697C>T
(ELN)
|
ENSP00000252034.7:p.Ala566Val
|
|
ENST00000320399.10:c.1697C>T
(ELN)
|
ENSP00000313565.6:p.Ala566Val
|
|
ENST00000320492.11:c.1454C>T
(ELN)
|
ENSP00000315607.7:p.Ala485Val
|
|
ENST00000357036.9:c.1712C>T
(ELN)
|
ENSP00000349540.5:p.Ala571Val
|
|
ENST00000358929.8:c.1784C>T
(ELN)
|
ENSP00000351807.5:p.Ala595Val
|
|
ENST00000380553.8:c.1289C>T
(ELN)
|
ENSP00000369926.4:p.Ala430Val
|
|
ENST00000380562.8:c.1715C>T
(ELN)
|
ENSP00000369936.4:p.Ala572Val
|
|
ENST00000380575.8:c.1610C>T
(ELN)
|
ENSP00000369949.4:p.Ala537Val
|
|
ENST00000380576.9:c.1640C>T
(ELN)
|
ENSP00000369950.5:p.Ala547Val
|
|
ENST00000380584.8:c.1553C>T
(ELN)
|
ENSP00000369958.4:p.Ala518Val
|
|
ENST00000414324.5:c.1625C>T
(ELN)
|
ENSP00000392575.1:p.Ala542Val
|
|
ENST00000429192.5:c.1655C>T
(ELN)
|
ENSP00000391129.1:p.Ala552Val
|
|
ENST00000445912.5:c.1697C>T
(ELN)
|
ENSP00000389857.1:p.Ala566Val
|
|
ENST00000458204.5:c.1667C>T
(ELN)
|
ENSP00000403162.1:p.Ala556Val
|
|
ENST00000621115.4:c.1430C>T
(ELN)
|
ENSP00000480955.1:p.Ala477Val
|
|
ENST00000692049.1:c.1784C>T
(ELN)
|
ENSP00000510104.1:p.Ala595Val
|
|
XM_005250187.1:c.1661C>T
(ELN)
|
XP_005250244.1:p.Ala554Val
|
|
XM_005250187.2:c.1661C>T
(ELN)
|
XP_005250244.1:p.Ala554Val
|
|
XM_005250188.1:c.1655C>T
(ELN)
|
XP_005250245.1:p.Ala552Val
|
|
XM_005250188.2:c.1655C>T
(ELN)
|
XP_005250245.1:p.Ala552Val
|
|
XM_011515868.1:c.1712C>T
(ELN)
|
XP_011514170.1:p.Ala571Val
|
|
XM_011515868.2:c.1712C>T
(ELN)
|
XP_011514170.1:p.Ala571Val
|
|
XM_011515869.1:c.1682C>T
(ELN)
|
XP_011514171.1:p.Ala561Val
|
|
XM_011515870.1:c.1676C>T
(ELN)
|
XP_011514172.1:p.Ala559Val
|
|
XM_011515871.1:c.1670C>T
(ELN)
|
XP_011514173.1:p.Ala557Val
|
|
XM_011515871.2:c.1670C>T
(ELN)
|
XP_011514173.1:p.Ala557Val
|
|
XM_011515872.1:c.1658C>T
(ELN)
|
XP_011514174.1:p.Ala553Val
|
|
XM_011515872.2:c.1658C>T
(ELN)
|
XP_011514174.1:p.Ala553Val
|
|
XM_011515873.1:c.1655C>T
(ELN)
|
XP_011514175.1:p.Ala552Val
|
|
XM_011515873.2:c.1655C>T
(ELN)
|
XP_011514175.1:p.Ala552Val
|
|
XM_011515874.1:c.1646C>T
(ELN)
|
XP_011514176.1:p.Ala549Val
|
|
XM_011515875.1:c.1631C>T
(ELN)
|
XP_011514177.1:p.Ala544Val
|
|
XM_011515875.2:c.1631C>T
(ELN)
|
XP_011514177.1:p.Ala544Val
|
|
XM_011515876.1:c.1712C>T
(ELN)
|
XP_011514178.1:p.Ala571Val
|
|
XM_011515876.2:c.1712C>T
(ELN)
|
XP_011514178.1:p.Ala571Val
|
|
XM_011515877.1:c.1601C>T
(ELN)
|
XP_011514179.1:p.Ala534Val
|
|
XM_011515877.2:c.1601C>T
(ELN)
|
XP_011514179.1:p.Ala534Val
|
|
XM_017011813.1:c.1625C>T
(ELN)
|
XP_016867302.1:p.Ala542Val
|
|
XM_017011814.2:c.1613C>T
(ELN)
|
XP_016867303.1:p.Ala538Val
|
|
XR_001745243.1:n.76-419G>A
(ELN-AS1)
|
|
