ENST00000682275.1:c.1741G>T
|
ENSP00000507852.1:p.Ala581Ser
|
|
ENST00000683395.1:c.1682G>T
|
|
|
ENST00000684087.1:c.1705G>T
|
ENSP00000506978.1:p.Ala569Ser
|
|
ENST00000506362.2:c.1456G>T
|
ENSP00000424103.2:p.Ala486Ser
|
|
ENST00000673642.1:c.1364G>T
|
ENSP00000501242.1:n.1364G>T
|
|
ENST00000673991.1:c.1741G>T
|
ENSP00000501033.1:p.Ala581Ser
|
|
ENST00000226760.5:c.1705G>T
MANE Select
|
ENSP00000226760.1:p.Ala569Ser
|
|
ENST00000503569.5:c.1705G>T
|
ENSP00000423337.1:p.Ala569Ser
|
|
ENST00000507765.1:n.1890G>T
|
|
|
NM_001145853.1:c.1705G>T
|
NP_001139325.1:p.Ala569Ser
|
|
NM_006005.3:c.1705G>T
MANE Select
|
NP_005996.2:p.Ala569Ser
|
|
XM_017008586.1:c.1714G>T
|
XP_016864075.1:p.Ala572Ser
|
|