ENST00000219794.11:c.453C>G
MANE Select
|
ENSP00000219794.6:p.Tyr151Ter
|
|
ENST00000219794.10:c.453C>G
|
ENSP00000219794.6:p.Tyr151Ter
|
|
ENST00000287507.7:c.453C>G
|
ENSP00000287507.3:p.Tyr151Ter
|
|
ENST00000394950.7:c.453C>G
|
ENSP00000378404.3:p.Tyr151Ter
|
|
ENST00000394951.5:c.453C>G
|
ENSP00000378405.1:p.Tyr151Ter
|
|
ENST00000484226.2:c.426C>G
|
ENSP00000457226.1:p.Tyr142Ter
|
|
ENST00000566568.1:n.954C>G
|
|
|
ENST00000567530.5:c.453C>G
|
ENSP00000456479.1:p.Tyr151Ter
|
|
NM_001122957.2:c.453C>G
|
NP_001116429.1:p.Tyr151Ter
|
|
NM_001271926.1:c.453C>G
|
NP_001258855.1:p.Tyr151Ter
|
|
NM_005881.3:c.453C>G
|
NP_005872.2:p.Tyr151Ter
|
|
XM_017022859.1:c.453C>G
|
XP_016878348.1:p.Tyr151Ter
|
|
NM_005881.4:c.453C>G
MANE Select
|
NP_005872.2:p.Tyr151Ter
|
|
NM_001122957.3:c.453C>G
|
NP_001116429.1:p.Tyr151Ter
|
|
NM_001271926.2:c.453C>G
|
NP_001258855.1:p.Tyr151Ter
|
|
NM_001122957.4:c.453C>G
|
NP_001116429.1:p.Tyr151Ter
|
|
NM_001271926.3:c.453C>G
|
NP_001258855.1:p.Tyr151Ter
|
|