ENST00000336411.7:c.1427T>G
|
ENSP00000337915.3:p.Met476Arg
|
|
ENST00000651162.1:n.769T>G
|
|
|
ENST00000651514.1:c.1334T>G
MANE Select
|
ENSP00000498939.1:p.Met445Arg
|
|
ENST00000651783.1:c.875T>G
|
ENSP00000498924.1:p.Met292Arg
|
|
ENST00000652018.1:c.1187T>G
|
ENSP00000498733.1:p.Met396Arg
|
|
ENST00000336411.6:c.1334T>G
|
ENSP00000337915.2:p.Met445Arg
|
|
ENST00000354593.6:c.884T>G
|
ENSP00000346607.2:p.Met295Arg
|
|
NM_001202855.2:c.1331T>G
|
NP_001189784.1:p.Met444Arg
|
|
NM_017460.5:c.1334T>G
|
NP_059488.2:p.Met445Arg
|
|
XM_011515841.1:c.1427T>G
|
XP_011514143.1:p.Met476Arg
|
|
XM_011515842.1:c.1424T>G
|
XP_011514144.1:p.Met475Arg
|
|
NM_017460.6:c.1334T>G
MANE Select
|
NP_059488.2:p.Met445Arg
|
|
NM_001202855.3:c.1331T>G
|
NP_001189784.1:p.Met444Arg
|
|