ENST00000298910.12:c.6407A=
MANE Select
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ENSP00000298910.7:p.Glu2136=
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|
ENST00000636518.1:c.204A=
|
|
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ENST00000679360.1:c.*5316A=
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ENSP00000505368.1:n.*5316A=
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|
ENST00000679532.1:c.2181A=
|
|
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ENST00000679683.1:c.197A=
|
|
|
ENST00000680018.1:c.1852A=
|
ENSP00000505347.1:n.1852A=
|
|
ENST00000680422.1:c.2052A=
|
|
|
ENST00000680425.1:c.1574A=
|
ENSP00000506459.1:n.1574A=
|
|
ENST00000680453.1:c.1864A=
|
|
|
ENST00000680790.1:c.6152A=
|
ENSP00000505335.1:p.Glu2051=
|
|
ENST00000681136.1:n.2391A=
|
|
|
ENST00000681696.1:c.2090A=
|
ENSP00000505871.1:p.Glu697=
|
|
ENST00000298910.11:c.6407A=
|
ENSP00000298910.7:p.Glu2136=
|
|
ENST00000430804.5:c.3703A=
|
|
|
ENST00000479187.5:n.3088A=
|
|
|
NM_198578.3:c.6407A=
|
NP_940980.3:p.Glu2136=
|
|
XM_005268629.2:c.6407A=
|
XP_005268686.1:p.Glu2136=
|
|
XM_011537877.1:c.6407A=
|
XP_011536179.1:p.Glu2136=
|
|
XM_011537878.1:c.6407A=
|
XP_011536180.1:p.Glu2136=
|
|
XM_011537879.1:c.5204A=
|
XP_011536181.1:p.Glu1735=
|
|
XM_005268629.4:c.6407A=
|
XP_005268686.1:p.Glu2136=
|
|
XM_011537877.3:c.6407A=
|
XP_011536179.1:p.Glu2136=
|
|
XM_017018787.1:c.3323A=
|
XP_016874276.1:p.Glu1108=
|
|
XM_017018788.2:c.2669A=
|
XP_016874277.1:p.Glu890=
|
|
XM_024448833.1:c.5204A=
|
XP_024304601.1:p.Glu1735=
|
|
NM_198578.4:c.6407A=
MANE Select
|
NP_940980.4:p.Glu2136=
|
|