ENST00000394817.7:c.1336T>A
MANE Select
|
ENSP00000378294.2:p.Phe446Ile
|
|
ENST00000265195.9:c.1336T>A
|
ENSP00000265195.5:p.Phe446Ile
|
|
ENST00000394817.6:c.1336T>A
|
ENSP00000378294.2:p.Phe446Ile
|
|
ENST00000509534.5:c.1357T>A
|
ENSP00000426858.1:p.Phe453Ile
|
|
ENST00000515008.1:n.671T>A
|
|
|
NM_001037633.1:c.1336T>A
|
NP_001032722.1:p.Phe446Ile
|
|
NM_022464.4:c.1336T>A
|
NP_071909.1:p.Phe446Ile
|
|
XM_011543570.1:c.1366T>A
|
XP_011541872.1:p.Phe456Ile
|
|
XM_011543570.2:c.1366T>A
|
XP_011541872.1:p.Phe456Ile
|
|
XM_024446164.1:c.1336T>A
|
XP_024301932.1:p.Phe446Ile
|
|
NM_022464.5:c.1336T>A
MANE Select
|
NP_071909.1:p.Phe446Ile
|
|
NM_001037633.2:c.1336T>A
|
NP_001032722.1:p.Phe446Ile
|
|