ENST00000298910.12:c.7181G>A
MANE Select
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ENSP00000298910.7:p.Arg2394Lys
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|
ENST00000636518.1:c.978G>A
|
|
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ENST00000679360.1:c.*6090G>A
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ENSP00000505368.1:n.*6090G>A
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|
ENST00000679532.1:c.2955G>A
|
|
|
ENST00000679683.1:c.971G>A
|
|
|
ENST00000680018.1:c.2626G>A
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ENSP00000505347.1:n.2626G>A
|
|
ENST00000680422.1:c.4268G>A
|
|
|
ENST00000680425.1:c.2348G>A
|
ENSP00000506459.1:n.2348G>A
|
|
ENST00000680453.1:c.2638G>A
|
|
|
ENST00000680790.1:c.6926G>A
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ENSP00000505335.1:p.Arg2309Lys
|
|
ENST00000681136.1:n.3165G>A
|
|
|
ENST00000681696.1:c.2864G>A
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ENSP00000505871.1:p.Arg955Lys
|
|
ENST00000681773.1:n.388G>A
|
|
|
ENST00000298910.11:c.7181G>A
|
ENSP00000298910.7:p.Arg2394Lys
|
|
ENST00000430804.5:c.4477G>A
|
|
|
ENST00000479187.5:n.3862G>A
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|
|
NM_198578.3:c.7181G>A
|
NP_940980.3:p.Arg2394Lys
|
|
XM_005268629.2:c.7181G>A
|
XP_005268686.1:p.Arg2394Lys
|
|
XM_011537877.1:c.7181G>A
|
XP_011536179.1:p.Arg2394Lys
|
|
XM_011537879.1:c.5978G>A
|
XP_011536181.1:p.Arg1993Lys
|
|
XR_944868.1:n.485-8727C>T
|
|
|
XM_005268629.4:c.7181G>A
|
XP_005268686.1:p.Arg2394Lys
|
|
XM_011537877.3:c.7181G>A
|
XP_011536179.1:p.Arg2394Lys
|
|
XM_017018787.1:c.4097G>A
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XP_016874276.1:p.Arg1366Lys
|
|
XM_017018788.2:c.3443G>A
|
XP_016874277.1:p.Arg1148Lys
|
|
XM_024448833.1:c.5978G>A
|
XP_024304601.1:p.Arg1993Lys
|
|
XR_944868.2:n.485-8727C>T
|
|
|
NM_198578.4:c.7181G>A
MANE Select
|
NP_940980.4:p.Arg2394Lys
|
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