ENST00000682275.1:c.1144G>T
|
ENSP00000507852.1:p.Ala382Ser
|
|
ENST00000683395.1:c.1085G>T
|
|
|
ENST00000684087.1:c.1108G>T
|
ENSP00000506978.1:p.Ala370Ser
|
|
ENST00000506362.2:c.859G>T
|
ENSP00000424103.2:p.Ala287Ser
|
|
ENST00000673642.1:c.767G>T
|
ENSP00000501242.1:p.Gly256Val
|
|
ENST00000673991.1:c.1144G>T
|
ENSP00000501033.1:p.Ala382Ser
|
|
ENST00000226760.5:c.1108G>T
MANE Select
|
ENSP00000226760.1:p.Ala370Ser
|
|
ENST00000503569.5:c.1108G>T
|
ENSP00000423337.1:p.Ala370Ser
|
|
ENST00000506362.1:c.741G>T
|
|
|
ENST00000507765.1:n.1293G>T
|
|
|
NM_001145853.1:c.1108G>T
|
NP_001139325.1:p.Ala370Ser
|
|
NM_006005.3:c.1108G>T
MANE Select
|
NP_005996.2:p.Ala370Ser
|
|
XM_017008586.1:c.1117G>T
|
XP_016864075.1:p.Ala373Ser
|
|