ENST00000298910.12:c.6463A>G
MANE Select
|
ENSP00000298910.7:p.Met2155Val
|
|
ENST00000636518.1:c.260A>G
|
|
|
ENST00000679360.1:c.*5372A>G
|
ENSP00000505368.1:n.*5372A>G
|
|
ENST00000679532.1:c.2237A>G
|
|
|
ENST00000679683.1:c.253A>G
|
|
|
ENST00000680018.1:c.1908A>G
|
ENSP00000505347.1:n.1908A>G
|
|
ENST00000680422.1:c.2108A>G
|
|
|
ENST00000680425.1:c.1630A>G
|
ENSP00000506459.1:n.1630A>G
|
|
ENST00000680453.1:c.1920A>G
|
|
|
ENST00000680790.1:c.6208A>G
|
ENSP00000505335.1:p.Met2070Val
|
|
ENST00000681136.1:n.2447A>G
|
|
|
ENST00000681696.1:c.2146A>G
|
ENSP00000505871.1:p.Met716Val
|
|
ENST00000298910.11:c.6463A>G
|
ENSP00000298910.7:p.Met2155Val
|
|
ENST00000430804.5:c.3759A>G
|
|
|
ENST00000479187.5:n.3144A>G
|
|
|
NM_198578.3:c.6463A>G
|
NP_940980.3:p.Met2155Val
|
|
XM_005268629.2:c.6463A>G
|
XP_005268686.1:p.Met2155Val
|
|
XM_011537877.1:c.6463A>G
|
XP_011536179.1:p.Met2155Val
|
|
XM_011537878.1:c.6463A>G
|
XP_011536180.1:p.Met2155Val
|
|
XM_011537879.1:c.5260A>G
|
XP_011536181.1:p.Met1754Val
|
|
XM_005268629.4:c.6463A>G
|
XP_005268686.1:p.Met2155Val
|
|
XM_011537877.3:c.6463A>G
|
XP_011536179.1:p.Met2155Val
|
|
XM_017018787.1:c.3379A>G
|
XP_016874276.1:p.Met1127Val
|
|
XM_017018788.2:c.2725A>G
|
XP_016874277.1:p.Met909Val
|
|
XM_024448833.1:c.5260A>G
|
XP_024304601.1:p.Met1754Val
|
|
NM_198578.4:c.6463A>G
MANE Select
|
NP_940980.4:p.Met2155Val
|
|