ENST00000474370.2:n.2422G=
|
|
|
ENST00000492391.2:n.1573G=
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|
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ENST00000682645.1:n.3520G=
|
|
|
ENST00000683432.1:c.*624G=
|
ENSP00000508174.1:n.*624G=
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|
ENST00000684207.1:c.449G=
|
ENSP00000506942.1:p.Arg150=
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|
ENST00000297157.8:c.449G=
MANE Select
|
ENSP00000297157.3:p.Arg150=
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|
ENST00000297157.7:c.449G=
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ENSP00000297157.3:p.Arg150=
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|
ENST00000448915.1:c.347G=
|
ENSP00000411577.1:p.Arg116=
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|
NM_203288.1:c.449G=
|
NP_976033.1:p.Arg150=
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|
XM_011515468.1:c.347G=
|
XP_011513770.1:p.Arg116=
|
|
XM_011515468.3:c.347G=
|
XP_011513770.1:p.Arg116=
|
|
NM_203288.2:c.449G=
MANE Select
|
NP_976033.1:p.Arg150=
|
|