ENST00000336411.7:c.1431G>A
|
ENSP00000337915.3:p.Arg477=
|
|
ENST00000651162.1:n.773G>A
|
|
|
ENST00000651514.1:c.1338G>A
MANE Select
|
ENSP00000498939.1:p.Arg446=
|
|
ENST00000651783.1:c.879G>A
|
ENSP00000498924.1:p.Arg293=
|
|
ENST00000652018.1:c.1191G>A
|
ENSP00000498733.1:p.Arg397=
|
|
ENST00000336411.6:c.1338G>A
|
ENSP00000337915.2:p.Arg446=
|
|
ENST00000354593.6:c.888G>A
|
ENSP00000346607.2:p.Arg296=
|
|
NM_001202855.2:c.1335G>A
|
NP_001189784.1:p.Arg445=
|
|
NM_017460.5:c.1338G>A
|
NP_059488.2:p.Arg446=
|
|
XM_011515841.1:c.1431G>A
|
XP_011514143.1:p.Arg477=
|
|
XM_011515842.1:c.1428G>A
|
XP_011514144.1:p.Arg476=
|
|
NM_017460.6:c.1338G>A
MANE Select
|
NP_059488.2:p.Arg446=
|
|
NM_001202855.3:c.1335G>A
|
NP_001189784.1:p.Arg445=
|
|