ENST00000262418.12:c.1944G=
MANE Select
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ENSP00000262418.6:p.Trp648=
|
|
ENST00000262418.10:c.1944G=
|
ENSP00000262418.6:p.Trp648=
|
|
ENST00000399246.3:c.846G=
|
ENSP00000382190.3:p.Trp282=
|
|
NM_000342.3:c.1944G=
|
NP_000333.1:p.Trp648=
|
|
XM_005257593.3:c.1749G=
|
XP_005257650.1:p.Trp583=
|
|
XM_011525129.1:c.1854G=
|
XP_011523431.1:p.Trp618=
|
|
XM_011525130.1:c.1944G=
|
XP_011523432.1:p.Trp648=
|
|
XM_011525131.1:c.1944G=
|
XP_011523433.1:p.Trp648=
|
|
XM_005257593.5:c.1749G=
|
XP_005257650.1:p.Trp583=
|
|
XM_011525129.2:c.1854G=
|
XP_011523431.1:p.Trp618=
|
|
NM_000342.4:c.1944G=
MANE Select
|
NP_000333.1:p.Trp648=
|
|