ENST00000336411.7:c.1412G>C
|
ENSP00000337915.3:p.Arg471Thr
|
|
ENST00000651162.1:n.754G>C
|
|
|
ENST00000651514.1:c.1319G>C
MANE Select
|
ENSP00000498939.1:p.Arg440Thr
|
|
ENST00000651783.1:c.860G>C
|
ENSP00000498924.1:p.Arg287Thr
|
|
ENST00000652018.1:c.1172G>C
|
ENSP00000498733.1:p.Arg391Thr
|
|
ENST00000336411.6:c.1319G>C
|
ENSP00000337915.2:p.Arg440Thr
|
|
ENST00000354593.6:c.869G>C
|
ENSP00000346607.2:p.Arg290Thr
|
|
NM_001202855.2:c.1316G>C
|
NP_001189784.1:p.Arg439Thr
|
|
NM_017460.5:c.1319G>C
|
NP_059488.2:p.Arg440Thr
|
|
XM_011515841.1:c.1412G>C
|
XP_011514143.1:p.Arg471Thr
|
|
XM_011515842.1:c.1409G>C
|
XP_011514144.1:p.Arg470Thr
|
|
NM_017460.6:c.1319G>C
MANE Select
|
NP_059488.2:p.Arg440Thr
|
|
NM_001202855.3:c.1316G>C
|
NP_001189784.1:p.Arg439Thr
|
|