ENST00000394817.7:c.1277A>G
MANE Select
|
ENSP00000378294.2:p.Gln426Arg
|
|
ENST00000265195.9:c.1277A>G
|
ENSP00000265195.5:p.Gln426Arg
|
|
ENST00000394817.6:c.1277A>G
|
ENSP00000378294.2:p.Gln426Arg
|
|
ENST00000509534.5:c.1298A>G
|
ENSP00000426858.1:p.Gln433Arg
|
|
ENST00000515008.1:n.612A>G
|
|
|
NM_001037633.1:c.1277A>G
|
NP_001032722.1:p.Gln426Arg
|
|
NM_022464.4:c.1277A>G
|
NP_071909.1:p.Gln426Arg
|
|
XM_011543570.1:c.1307A>G
|
XP_011541872.1:p.Gln436Arg
|
|
XM_011543570.2:c.1307A>G
|
XP_011541872.1:p.Gln436Arg
|
|
XM_024446164.1:c.1277A>G
|
XP_024301932.1:p.Gln426Arg
|
|
NM_022464.5:c.1277A>G
MANE Select
|
NP_071909.1:p.Gln426Arg
|
|
NM_001037633.2:c.1277A>G
|
NP_001032722.1:p.Gln426Arg
|
|