ENST00000264595.7:c.738T>G
MANE Select
|
ENSP00000264595.2:p.Tyr246Ter
|
|
ENST00000264595.6:c.738T>G
|
ENSP00000264595.2:p.Tyr246Ter
|
|
ENST00000502310.5:c.309T>G
|
ENSP00000423798.1:p.Tyr103Ter
|
|
ENST00000506853.5:n.696T>G
|
|
|
ENST00000510635.1:c.404T>G
|
|
|
NM_000027.3:c.738T>G
|
NP_000018.2:p.Tyr246Ter
|
|
NM_001171988.1:c.708T>G
|
NP_001165459.1:p.Tyr236Ter
|
|
NR_033655.1:n.790T>G
|
|
|
XM_006714123.2:c.*32T>G
|
XP_006714186.1:n.*32T>G
|
|
XR_001741155.2:n.810T>G
|
|
|
NM_000027.4:c.738T>G
MANE Select
|
NP_000018.2:p.Tyr246Ter
|
|
NM_001171988.2:c.708T>G
|
NP_001165459.1:p.Tyr236Ter
|
|
NR_033655.2:n.724T>G
|
|
|