ENST00000298910.12:c.6426A>G
MANE Select
|
ENSP00000298910.7:p.Arg2142=
|
|
ENST00000636518.1:c.223A>G
|
|
|
ENST00000679360.1:c.*5335A>G
|
ENSP00000505368.1:n.*5335A>G
|
|
ENST00000679532.1:c.2200A>G
|
|
|
ENST00000679683.1:c.216A>G
|
|
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ENST00000680018.1:c.1871A>G
|
ENSP00000505347.1:n.1871A>G
|
|
ENST00000680422.1:c.2071A>G
|
|
|
ENST00000680425.1:c.1593A>G
|
ENSP00000506459.1:n.1593A>G
|
|
ENST00000680453.1:c.1883A>G
|
|
|
ENST00000680790.1:c.6171A>G
|
ENSP00000505335.1:p.Arg2057=
|
|
ENST00000681136.1:n.2410A>G
|
|
|
ENST00000681696.1:c.2109A>G
|
ENSP00000505871.1:p.Arg703=
|
|
ENST00000298910.11:c.6426A>G
|
ENSP00000298910.7:p.Arg2142=
|
|
ENST00000430804.5:c.3722A>G
|
|
|
ENST00000479187.5:n.3107A>G
|
|
|
NM_198578.3:c.6426A>G
|
NP_940980.3:p.Arg2142=
|
|
XM_005268629.2:c.6426A>G
|
XP_005268686.1:p.Arg2142=
|
|
XM_011537877.1:c.6426A>G
|
XP_011536179.1:p.Arg2142=
|
|
XM_011537878.1:c.6426A>G
|
XP_011536180.1:p.Arg2142=
|
|
XM_011537879.1:c.5223A>G
|
XP_011536181.1:p.Arg1741=
|
|
XM_005268629.4:c.6426A>G
|
XP_005268686.1:p.Arg2142=
|
|
XM_011537877.3:c.6426A>G
|
XP_011536179.1:p.Arg2142=
|
|
XM_017018787.1:c.3342A>G
|
XP_016874276.1:p.Arg1114=
|
|
XM_017018788.2:c.2688A>G
|
XP_016874277.1:p.Arg896=
|
|
XM_024448833.1:c.5223A>G
|
XP_024304601.1:p.Arg1741=
|
|
NM_198578.4:c.6426A>G
MANE Select
|
NP_940980.4:p.Arg2142=
|
|