ENST00000650793.2:n.312C>G
|
|
|
ENST00000697612.1:n.990C>G
|
|
|
ENST00000374881.3:c.279C>G
|
ENSP00000364015.2:p.Tyr93Ter
|
|
ENST00000374882.8:c.291C>G
MANE Select
|
ENSP00000364016.4:p.Tyr97Ter
|
|
ENST00000650411.1:n.1612C>G
|
|
|
ENST00000650793.1:n.312C>G
|
|
|
ENST00000374881.2:c.279C>G
|
ENSP00000364015.2:p.Tyr93Ter
|
|
ENST00000374882.7:c.291C>G
|
ENSP00000364016.3:p.Tyr97Ter
|
|
ENST00000395339.7:c.291C>G
|
ENSP00000378748.3:p.Tyr97Ter
|
|
ENST00000484003.1:n.517C>G
|
|
|
NM_004159.4:c.279C>G
|
NP_004150.1:p.Tyr93Ter
|
|
NM_148919.3:c.291C>G
|
NP_683720.2:p.Tyr97Ter
|
|
NM_148919.4:c.291C>G
MANE Select
|
NP_683720.2:p.Tyr97Ter
|
|
NM_004159.5:c.279C>G
|
NP_004150.1:p.Tyr93Ter
|
|