ENST00000496887.7:c.645G>T
|
ENSP00000434560.2:p.Ala215=
|
|
ENST00000646564.2:c.478-10464G>T
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ENSP00000495806.2:n.478-10464G>T
|
|
ENST00000155840.12:c.906G>T
MANE Select
|
ENSP00000155840.2:p.Ala302=
|
|
ENST00000335475.6:c.525G>T
|
ENSP00000334497.5:p.Ala175=
|
|
ENST00000646564.1:c.124-10464G>T
|
ENSP00000495806.1:n.124-10464G>T
|
|
ENST00000155840.9:c.906G>T
|
ENSP00000155840.2:p.Ala302=
|
|
ENST00000335475.5:c.525G>T
|
ENSP00000334497.5:p.Ala175=
|
|
NM_000218.2:c.906G>T , LRG_287t1:c.906G>T
|
NP_000209.2:p.Ala302=
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NM_181798.1:c.525G>T , LRG_287t2:c.525G>T
|
NP_861463.1:p.Ala175=
|
|
NM_000218.3:c.906G>T
MANE Select
|
NP_000209.2:p.Ala302=
|
|