ENST00000651671.1:c.1395C>G
MANE Select
|
ENSP00000498587.1:p.Ala465=
|
|
ENST00000679595.1:c.1395C>G
|
ENSP00000506241.1:p.Ala465=
|
|
ENST00000680133.1:c.1395C>G
|
ENSP00000505319.1:p.Ala465=
|
|
ENST00000680218.1:c.1395C>G
|
ENSP00000505339.1:p.Ala465=
|
|
ENST00000680668.1:c.1395C>G
|
ENSP00000506336.1:p.Ala465=
|
|
ENST00000680924.1:c.1395C>G
|
ENSP00000506031.1:p.Ala465=
|
|
ENST00000681135.1:c.1395C>G
|
ENSP00000506636.1:p.Ala465=
|
|
ENST00000681454.1:c.*631C>G
|
ENSP00000505763.1:n.*631C>G
|
|
ENST00000277541.6:c.1395C>G
|
ENSP00000277541.6:p.Ala465=
|
|
NM_017617.3:c.1395C>G
|
NP_060087.3:p.Ala465=
|
|
XM_011518717.1:c.696C>G
|
XP_011517019.1:p.Ala232=
|
|
NM_017617.5:c.1395C>G
MANE Select
|
NP_060087.3:p.Ala465=
|
|
XM_011518717.2:c.672C>G
|
XP_011517019.2:p.Ala224=
|
|