ENST00000687154.1:n.515-2074G>T
|
|
|
ENST00000688001.1:c.1369G>T
|
ENSP00000508987.1:p.Ala457Ser
|
|
ENST00000689296.1:c.1369G>T
|
ENSP00000510609.1:p.Ala457Ser
|
|
ENST00000689740.1:c.1417G>T
|
ENSP00000510300.1:p.Ala473Ser
|
|
ENST00000693680.1:c.1417G>T
|
ENSP00000509539.1:p.Ala473Ser
|
|
ENST00000361373.9:c.1558G>T
MANE Select
|
ENSP00000355296.3:p.Ala520Ser
|
|
ENST00000429277.7:c.1228G>T
|
ENSP00000401437.3:p.Ala410Ser
|
|
ENST00000623056.4:c.1573G>T
|
ENSP00000485500.1:p.Ala525Ser
|
|
ENST00000263066.10:c.1228G>T
|
ENSP00000263066.6:p.Ala410Ser
|
|
ENST00000361373.8:c.1558G>T
|
ENSP00000355296.3:p.Ala520Ser
|
|
ENST00000429277.6:c.1573G>T
|
ENSP00000401437.2:p.Ala525Ser
|
|
ENST00000623056.3:c.1573G>T
|
ENSP00000485500.1:p.Ala525Ser
|
|
NM_001080114.1:c.1228G>T
|
NP_001073583.1:p.Ala410Ser
|
|
NM_001171610.1:c.1573G>T
|
NP_001165081.1:p.Ala525Ser
|
|
NM_007078.2:c.1558G>T , LRG_385t1:c.1558G>T
|
NP_009009.1:p.Ala520Ser
|
|
XM_005269464.3:c.1558G>T
|
XP_005269521.1:p.Ala520Ser
|
|
XM_005269466.3:c.1369G>T
|
XP_005269523.1:p.Ala457Ser
|
|
XM_011539184.1:c.1810G>T
|
XP_011537486.1:p.Ala604Ser
|
|
XM_011539185.1:c.1810G>T
|
XP_011537487.1:p.Ala604Ser
|
|
XM_011539186.1:c.1762G>T
|
XP_011537488.1:p.Ala588Ser
|
|
XM_011539187.1:c.1621G>T
|
XP_011537489.1:p.Ala541Ser
|
|
XM_011539188.1:c.1606G>T
|
XP_011537490.1:p.Ala536Ser
|
|
XM_011539189.1:c.1465G>T
|
XP_011537491.1:p.Ala489Ser
|
|
XM_011539190.1:c.1417G>T
|
XP_011537492.1:p.Ala473Ser
|
|
XM_011539191.1:c.1276G>T
|
XP_011537493.1:p.Ala426Ser
|
|
XM_011539192.1:c.1261G>T
|
XP_011537494.1:p.Ala421Ser
|
|
XM_011539193.1:c.766G>T
|
XP_011537495.1:p.Ala256Ser
|
|
XM_011539194.1:c.577G>T
|
XP_011537496.1:p.Ala193Ser
|
|
XM_005269464.4:c.1558G>T
|
XP_005269521.1:p.Ala520Ser
|
|
XM_005269466.4:c.1369G>T
|
XP_005269523.1:p.Ala457Ser
|
|
XM_011539184.2:c.1810G>T
|
XP_011537486.1:p.Ala604Ser
|
|
XM_011539185.2:c.1810G>T
|
XP_011537487.1:p.Ala604Ser
|
|
XM_011539186.2:c.1762G>T
|
XP_011537488.1:p.Ala588Ser
|
|
XM_011539187.2:c.1621G>T
|
XP_011537489.1:p.Ala541Ser
|
|
XM_011539188.2:c.1606G>T
|
XP_011537490.1:p.Ala536Ser
|
|
XM_011539190.2:c.1417G>T
|
XP_011537492.1:p.Ala473Ser
|
|
XM_011539191.2:c.1276G>T
|
XP_011537493.1:p.Ala426Ser
|
|
XM_017015606.1:c.1606G>T
|
XP_016871095.1:p.Ala536Ser
|
|
XM_017015607.1:c.766G>T
|
XP_016871096.1:p.Ala256Ser
|
|
XM_024447785.1:c.1465G>T
|
XP_024303553.1:p.Ala489Ser
|
|
XM_024447786.1:c.1228G>T
|
XP_024303554.1:p.Ala410Ser
|
|
NM_001080114.2:c.1228G>T
|
NP_001073583.1:p.Ala410Ser
|
|
NM_001171610.2:c.1573G>T
|
NP_001165081.1:p.Ala525Ser
|
|
NM_001368064.1:c.1369G>T
|
NP_001354993.1:p.Ala457Ser
|
|
NM_001368065.1:c.1369G>T
|
NP_001354994.1:p.Ala457Ser
|
|
NM_001368066.1:c.1417G>T
|
NP_001354995.1:p.Ala473Ser
|
|
NM_007078.3:c.1558G>T
MANE Select
|
NP_009009.1:p.Ala520Ser
|
|