ENST00000420175.3:c.563G=
MANE Select
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ENSP00000391137.2:p.Cys188=
|
|
ENST00000275838.5:c.563G=
|
ENSP00000275838.1:p.Cys188=
|
|
ENST00000377867.7:c.518G=
|
ENSP00000367098.3:p.Cys173=
|
|
ENST00000420175.2:c.563G=
|
ENSP00000391137.2:p.Cys188=
|
|
NM_001142459.1:c.563G=
|
NP_001135931.2:p.Cys188=
|
|
NM_001142460.1:c.563G=
|
NP_001135932.2:p.Cys188=
|
|
NM_080871.3:c.518G=
|
NP_543147.2:p.Cys173=
|
|
XM_005249949.3:c.698G=
|
XP_005250006.1:p.Cys233=
|
|
NM_001142459.2:c.563G=
MANE Select
|
NP_001135931.2:p.Cys188=
|
|
NM_080871.4:c.518G=
|
NP_543147.2:p.Cys173=
|
|