ENST00000333371.8:c.-341T>G
MANE Select
|
ENSP00000327650.4:n.-341T>G
|
|
ENST00000333371.7:c.-341T>G
|
ENSP00000327650.3:n.-341T>G
|
|
ENST00000535906.1:c.-341T>G
|
ENSP00000444053.1:n.-341T>G
|
|
ENST00000556096.6:n.14T>G
|
|
|
ENST00000557358.1:n.7T>G
|
|
|
NM_001289148.1:c.-341T>G
|
NP_001276077.1:n.-341T>G
|
|
NM_001289149.1:c.-552T>G
|
NP_001276078.1:n.-552T>G
|
|
NM_018668.4:c.-341T>G , LRG_884t1:c.-341T>G
|
NP_061138.3:n.-341T>G
|
|
XM_005254887.1:c.-471T>G
|
XP_005254944.1:n.-471T>G
|
|
XM_011521448.1:c.-654T>G
|
XP_011519750.1:n.-654T>G
|
|
XM_017022075.2:c.-702T>G
|
XP_016877564.1:n.-702T>G
|
|
XM_017022076.1:c.-559T>G
|
XP_016877565.1:n.-559T>G
|
|
NM_018668.5:c.-341T>G
MANE Select
|
NP_061138.3:n.-341T>G
|
|