ENST00000597921.6:c.572G>A
MANE Select
|
ENSP00000471974.1:p.Cys191Tyr
|
|
ENST00000346664.9:c.572G>A
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ENSP00000264072.6:p.Cys191Tyr
|
|
ENST00000360067.8:c.569G>A
|
ENSP00000353178.4:p.Cys190Tyr
|
|
ENST00000597312.5:n.1097G>A
|
|
|
ENST00000597921.5:c.572G>A
|
ENSP00000471974.1:p.Cys191Tyr
|
|
ENST00000597934.1:n.934G>A
|
|
|
ENST00000598803.5:n.1067G>A
|
|
|
NM_001207019.2:c.569G>A
|
NP_001193948.2:p.Cys190Tyr
|
|
NM_001220500.1:c.572G>A
|
NP_001207429.1:p.Cys191Tyr
|
|
NM_002002.4:c.572G>A
|
NP_001993.2:p.Cys191Tyr
|
|
XM_005272462.3:c.572G>A
|
XP_005272519.1:p.Cys191Tyr
|
|
XM_005272462.4:c.572G>A
|
XP_005272519.1:p.Cys191Tyr
|
|
NM_001220500.2:c.572G>A
MANE Select
|
NP_001207429.1:p.Cys191Tyr
|
|
NM_001207019.3:c.569G>A
|
NP_001193948.2:p.Cys190Tyr
|
|
NM_002002.5:c.572G>A
|
NP_001993.2:p.Cys191Tyr
|
|