ENST00000298910.12:c.6498C>T
MANE Select
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ENSP00000298910.7:p.Ser2166=
|
|
ENST00000636518.1:c.295C>T
|
|
|
ENST00000679360.1:c.*5407C>T
|
ENSP00000505368.1:n.*5407C>T
|
|
ENST00000679532.1:c.2272C>T
|
|
|
ENST00000679683.1:c.288C>T
|
|
|
ENST00000680018.1:c.1943C>T
|
ENSP00000505347.1:n.1943C>T
|
|
ENST00000680422.1:c.2143C>T
|
|
|
ENST00000680425.1:c.1665C>T
|
ENSP00000506459.1:n.1665C>T
|
|
ENST00000680453.1:c.1955C>T
|
|
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ENST00000680790.1:c.6243C>T
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ENSP00000505335.1:p.Ser2081=
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ENST00000681136.1:n.2482C>T
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ENST00000681696.1:c.2181C>T
|
ENSP00000505871.1:p.Ser727=
|
|
ENST00000298910.11:c.6498C>T
|
ENSP00000298910.7:p.Ser2166=
|
|
ENST00000430804.5:c.3794C>T
|
|
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ENST00000479187.5:n.3179C>T
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|
NM_198578.3:c.6498C>T
|
NP_940980.3:p.Ser2166=
|
|
XM_005268629.2:c.6498C>T
|
XP_005268686.1:p.Ser2166=
|
|
XM_011537877.1:c.6498C>T
|
XP_011536179.1:p.Ser2166=
|
|
XM_011537878.1:c.6498C>T
|
XP_011536180.1:p.Ser2166=
|
|
XM_011537879.1:c.5295C>T
|
XP_011536181.1:p.Ser1765=
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|
XM_005268629.4:c.6498C>T
|
XP_005268686.1:p.Ser2166=
|
|
XM_011537877.3:c.6498C>T
|
XP_011536179.1:p.Ser2166=
|
|
XM_017018787.1:c.3414C>T
|
XP_016874276.1:p.Ser1138=
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XM_017018788.2:c.2760C>T
|
XP_016874277.1:p.Ser920=
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|
XM_024448833.1:c.5295C>T
|
XP_024304601.1:p.Ser1765=
|
|
NM_198578.4:c.6498C>T
MANE Select
|
NP_940980.4:p.Ser2166=
|
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