ENST00000336411.7:c.1495T>C
|
ENSP00000337915.3:p.Cys499Arg
|
|
ENST00000651162.1:n.837T>C
|
|
|
ENST00000651514.1:c.1402T>C
MANE Select
|
ENSP00000498939.1:p.Cys468Arg
|
|
ENST00000651783.1:c.943T>C
|
ENSP00000498924.1:p.Cys315Arg
|
|
ENST00000652018.1:c.1255T>C
|
ENSP00000498733.1:p.Cys419Arg
|
|
ENST00000336411.6:c.1402T>C
|
ENSP00000337915.2:p.Cys468Arg
|
|
ENST00000354593.6:c.952T>C
|
ENSP00000346607.2:p.Cys318Arg
|
|
NM_001202855.2:c.1399T>C
|
NP_001189784.1:p.Cys467Arg
|
|
NM_017460.5:c.1402T>C
|
NP_059488.2:p.Cys468Arg
|
|
XM_011515841.1:c.1495T>C
|
XP_011514143.1:p.Cys499Arg
|
|
XM_011515842.1:c.1492T>C
|
XP_011514144.1:p.Cys498Arg
|
|
NM_017460.6:c.1402T>C
MANE Select
|
NP_059488.2:p.Cys468Arg
|
|
NM_001202855.3:c.1399T>C
|
NP_001189784.1:p.Cys467Arg
|
|