ENST00000496887.7:c.710T>C
|
ENSP00000434560.2:p.Val237Ala
|
|
ENST00000646564.2:c.527T>C
|
ENSP00000495806.2:p.Val176Ala
|
|
ENST00000155840.12:c.971T>C
MANE Select
|
ENSP00000155840.2:p.Val324Ala
|
|
ENST00000335475.6:c.590T>C
|
ENSP00000334497.5:p.Val197Ala
|
|
ENST00000646564.1:c.173T>C
|
ENSP00000495806.1:p.Val58Ala
|
|
ENST00000155840.9:c.971T>C
|
ENSP00000155840.2:p.Val324Ala
|
|
ENST00000335475.5:c.590T>C
|
ENSP00000334497.5:p.Val197Ala
|
|
NM_000218.2:c.971T>C , LRG_287t1:c.971T>C
|
NP_000209.2:p.Val324Ala
|
|
NM_181798.1:c.590T>C , LRG_287t2:c.590T>C
|
NP_861463.1:p.Val197Ala
|
|
NM_000218.3:c.971T>C
MANE Select
|
NP_000209.2:p.Val324Ala
|
|