ENST00000298910.12:c.7115T>C
MANE Select
|
ENSP00000298910.7:p.Val2372Ala
|
|
ENST00000636518.1:c.912T>C
|
|
|
ENST00000679360.1:c.*6024T>C
|
ENSP00000505368.1:n.*6024T>C
|
|
ENST00000679532.1:c.2889T>C
|
|
|
ENST00000679683.1:c.905T>C
|
|
|
ENST00000680018.1:c.2560T>C
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ENSP00000505347.1:n.2560T>C
|
|
ENST00000680422.1:c.4202T>C
|
|
|
ENST00000680425.1:c.2282T>C
|
ENSP00000506459.1:n.2282T>C
|
|
ENST00000680453.1:c.2572T>C
|
|
|
ENST00000680790.1:c.6860T>C
|
ENSP00000505335.1:p.Val2287Ala
|
|
ENST00000681136.1:n.3099T>C
|
|
|
ENST00000681696.1:c.2798T>C
|
ENSP00000505871.1:p.Val933Ala
|
|
ENST00000681773.1:n.322T>C
|
|
|
ENST00000298910.11:c.7115T>C
|
ENSP00000298910.7:p.Val2372Ala
|
|
ENST00000430804.5:c.4411T>C
|
|
|
ENST00000479187.5:n.3796T>C
|
|
|
NM_198578.3:c.7115T>C
|
NP_940980.3:p.Val2372Ala
|
|
XM_005268629.2:c.7115T>C
|
XP_005268686.1:p.Val2372Ala
|
|
XM_011537877.1:c.7115T>C
|
XP_011536179.1:p.Val2372Ala
|
|
XM_011537879.1:c.5912T>C
|
XP_011536181.1:p.Val1971Ala
|
|
XR_944868.1:n.485-8661A>G
|
|
|
XM_005268629.4:c.7115T>C
|
XP_005268686.1:p.Val2372Ala
|
|
XM_011537877.3:c.7115T>C
|
XP_011536179.1:p.Val2372Ala
|
|
XM_017018787.1:c.4031T>C
|
XP_016874276.1:p.Val1344Ala
|
|
XM_017018788.2:c.3377T>C
|
XP_016874277.1:p.Val1126Ala
|
|
XM_024448833.1:c.5912T>C
|
XP_024304601.1:p.Val1971Ala
|
|
XR_944868.2:n.485-8661A>G
|
|
|
NM_198578.4:c.7115T>C
MANE Select
|
NP_940980.4:p.Val2372Ala
|
|