ENST00000336411.7:c.1347A>T
|
ENSP00000337915.3:p.Ile449=
|
|
ENST00000651162.1:n.689A>T
|
|
|
ENST00000651514.1:c.1254A>T
MANE Select
|
ENSP00000498939.1:p.Arg418Ser
|
|
ENST00000651783.1:c.795A>T
|
ENSP00000498924.1:p.Arg265Ser
|
|
ENST00000652018.1:c.1107A>T
|
ENSP00000498733.1:p.Arg369Ser
|
|
ENST00000336411.6:c.1254A>T
|
ENSP00000337915.2:p.Arg418Ser
|
|
ENST00000354593.6:c.804A>T
|
ENSP00000346607.2:p.Arg268Ser
|
|
NM_001202855.2:c.1251A>T
|
NP_001189784.1:p.Arg417Ser
|
|
NM_017460.5:c.1254A>T
|
NP_059488.2:p.Arg418Ser
|
|
XM_011515841.1:c.1347A>T
|
XP_011514143.1:p.Ile449=
|
|
XM_011515842.1:c.1344A>T
|
XP_011514144.1:p.Ile448=
|
|
NM_017460.6:c.1254A>T
MANE Select
|
NP_059488.2:p.Arg418Ser
|
|
NM_001202855.3:c.1251A>T
|
NP_001189784.1:p.Arg417Ser
|
|