|
NM_018979.4:c.3698C>T
MANE Select
|
NP_061852.3:p.Ala1233Val
|
|
ENST00000315939.11:c.3698C>T
MANE Select
|
ENSP00000313059.6:p.Ala1233Val
|
|
NM_213655.5:c.4454C>T
MANE Plus Clinical
|
NP_998820.3:p.Ala1485Val
|
|
ENST00000340908.9:c.4454C>T
MANE Plus Clinical
|
ENSP00000341292.5:p.Ala1485Val
|
|
NM_001184985.1:c.4478C>T
|
NP_001171914.1:p.Ala1493Val
|
|
NM_001184985.2:c.4478C>T
|
NP_001171914.1:p.Ala1493Val
|
|
NM_014823.2:c.2957C>T
|
NP_055638.2:p.Ala986Val
|
|
NM_014823.3:c.2957C>T
|
NP_055638.2:p.Ala986Val
|
|
NM_018979.3:c.3698C>T
|
NP_061852.3:p.Ala1233Val
|
|
NM_213655.4:c.4454C>T
|
NP_998820.3:p.Ala1485Val
|
|
ENST00000315939.10:c.3698C>T
|
ENSP00000313059.6:p.Ala1233Val
|
|
ENST00000340908.8:c.4454C>T
|
ENSP00000341292.5:p.Ala1485Val
|
|
ENST00000530271.6:c.4937C>T
|
ENSP00000433548.3:p.Ala1646Val
|
|
ENST00000534872.1:c.398C>T
|
ENSP00000446253.1:p.Ala133Val
|
|
ENST00000535572.5:c.2957C>T
|
ENSP00000441972.1:p.Ala986Val
|
|
ENST00000537687.5:c.4478C>T
|
ENSP00000444465.1:p.Ala1493Val
|
|
ENST00000674810.1:n.4295C>T
|
|
|
ENST00000675236.1:n.2593C>T
|
|
|
ENST00000675631.1:c.2477C>T
|
ENSP00000502415.1:p.Ala826Val
|
|
ENST00000676347.1:c.1145C>T
|
ENSP00000501875.1:p.Ala382Val
|
|
XM_006719003.1:c.3695C>T
|
XP_006719066.1:p.Ala1232Val
|
|
XM_006719003.2:c.3695C>T
|
XP_006719066.1:p.Ala1232Val
|
|
XM_011520997.1:c.4937C>T
|
XP_011519299.1:p.Ala1646Val
|
|
XM_011520997.3:c.4937C>T
|
XP_011519299.1:p.Ala1646Val
|
|
XM_011520998.1:c.4934C>T
|
XP_011519300.1:p.Ala1645Val
|
|
XM_011520998.2:c.4934C>T
|
XP_011519300.1:p.Ala1645Val
|
|
XM_011520999.1:c.4937C>T
|
XP_011519301.1:p.Ala1646Val
|
|
XM_011520999.2:c.4937C>T
|
XP_011519301.1:p.Ala1646Val
|
|
XM_011521000.1:c.4937C>T
|
XP_011519302.1:p.Ala1646Val
|
|
XM_011521000.2:c.4937C>T
|
XP_011519302.1:p.Ala1646Val
|
|
XM_011521001.1:c.4658C>T
|
XP_011519303.1:p.Ala1553Val
|
|
XM_011521001.2:c.4658C>T
|
XP_011519303.1:p.Ala1553Val
|
|
XM_011521002.1:c.4475C>T
|
XP_011519304.1:p.Ala1492Val
|
|
XM_011521002.2:c.4475C>T
|
XP_011519304.1:p.Ala1492Val
|
|
XM_011521003.1:c.4199C>T
|
XP_011519305.1:p.Ala1400Val
|
|
XM_011521003.2:c.4199C>T
|
XP_011519305.1:p.Ala1400Val
|
|
XM_011521004.1:c.4196C>T
|
XP_011519306.1:p.Ala1399Val
|
|
XM_011521004.2:c.4196C>T
|
XP_011519306.1:p.Ala1399Val
|
|
XM_011521005.1:c.3716C>T
|
XP_011519307.1:p.Ala1239Val
|
|
XM_011521005.2:c.3716C>T
|
XP_011519307.1:p.Ala1239Val
|
|
XM_011521006.1:c.3614C>T
|
XP_011519308.1:p.Ala1205Val
|
|
XM_011521006.2:c.3614C>T
|
XP_011519308.1:p.Ala1205Val
|
|
XM_011521007.1:c.3611C>T
|
XP_011519309.1:p.Ala1204Val
|
|
XM_011521007.2:c.3611C>T
|
XP_011519309.1:p.Ala1204Val
|
|
XM_011521008.1:c.2876C>T
|
XP_011519310.1:p.Ala959Val
|
|
XM_011521008.2:c.2876C>T
|
XP_011519310.1:p.Ala959Val
|
|
XM_011521009.1:c.2873C>T
|
XP_011519311.1:p.Ala958Val
|
|
XM_011521009.2:c.2873C>T
|
XP_011519311.1:p.Ala958Val
|
|
XM_017019834.1:c.3236C>T
|
XP_016875323.1:p.Ala1079Val
|
|
XM_017019835.1:c.3155C>T
|
XP_016875324.1:p.Ala1052Val
|
|
XM_017019836.1:c.3152C>T
|
XP_016875325.1:p.Ala1051Val
|
|
XM_017019837.1:c.2960C>T
|
XP_016875326.1:p.Ala987Val
|
|
XM_017019838.1:c.2957C>T
|
XP_016875327.1:p.Ala986Val
|
|
XM_017019839.1:c.2876C>T
|
XP_016875328.1:p.Ala959Val
|
