ENST00000394975.3:c.362C>G
MANE Select
|
ENSP00000378426.2:p.Ala121Gly
|
|
ENST00000300851.10:c.423C>G
|
ENSP00000300851.6:p.Gly141=
|
|
ENST00000319788.11:c.444C>G
|
ENSP00000326135.7:p.Gly148=
|
|
ENST00000354895.4:c.252C>G
|
ENSP00000346969.4:p.Gly84=
|
|
ENST00000394971.7:c.456C>G
|
ENSP00000378422.3:p.Gly152=
|
|
ENST00000394975.2:c.362C>G
|
ENSP00000378426.2:p.Ala121Gly
|
|
ENST00000420057.2:c.324C>G
|
|
|
ENST00000472468.1:c.47C>G
|
ENSP00000458994.1:p.Ala16Gly
|
|
ENST00000498155.1:c.459C>G
|
ENSP00000417662.1:p.Gly153=
|
|
ENST00000529564.1:c.283+2048C>G
|
ENSP00000431371.1:n.283+2048C>G
|
|
ENST00000532364.1:c.173+3293C>G
|
ENSP00000460316.1:n.173+3293C>G
|
|
ENST00000533518.5:c.235C>G
|
|
|
NM_001311311.1:c.446C>G
|
NP_001298240.1:p.Ala149Gly
|
|
NM_024006.4:c.362C>G
|
NP_076869.1:p.Ala121Gly
|
|
NM_024006.5:c.362C>G
|
NP_076869.1:p.Ala121Gly
|
|
NM_206824.1:c.252C>G
|
NP_996560.1:p.Gly84=
|
|
NM_206824.2:c.252C>G
|
NP_996560.1:p.Gly84=
|
|
XM_011545944.1:c.362C>G
|
XP_011544246.1:p.Ala121Gly
|
|
XM_011545945.1:c.252C>G
|
XP_011544247.1:p.Gly84=
|
|
XR_950848.1:n.1150C>G
|
|
|
NM_024006.6:c.362C>G
MANE Select
|
NP_076869.1:p.Ala121Gly
|
|
NM_001311311.2:c.446C>G
|
NP_001298240.1:p.Ala149Gly
|
|
NM_206824.3:c.252C>G
|
NP_996560.1:p.Gly84=
|
|