ENST00000695651.1:n.2571T>C
|
|
|
ENST00000695653.1:c.2132T>C
|
ENSP00000512084.1:p.Met711Thr
|
|
ENST00000695654.1:c.3248T>C
|
ENSP00000512085.1:p.Met1083Thr
|
|
ENST00000695689.1:c.194T>C
|
ENSP00000512101.1:n.194T>C
|
|
ENST00000695690.1:n.414T>C
|
|
|
ENST00000695691.1:n.414T>C
|
|
|
ENST00000245907.11:c.4223T>C
MANE Select
|
ENSP00000245907.4:p.Met1408Thr
|
|
ENST00000245907.10:c.4223T>C
|
ENSP00000245907.4:p.Met1408Thr
|
|
ENST00000596548.1:c.344T>C
|
ENSP00000469744.1:p.Met115Thr
|
|
ENST00000599899.5:n.1182T>C
|
|
|
ENST00000601008.1:c.242-4221T>C
|
ENSP00000471384.1:n.242-4221T>C
|
|
NM_000064.3:c.4223T>C
|
NP_000055.2:p.Met1408Thr
|
|
NM_000064.4:c.4223T>C
MANE Select
|
NP_000055.2:p.Met1408Thr
|
|