ENST00000547103.7:c.6236G>A
MANE Select
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ENSP00000447211.2:p.Cys2079Tyr
|
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ENST00000642294.1:c.176G>A
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ENSP00000493572.1:p.Cys59Tyr
|
|
ENST00000646859.1:c.6101G>A
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ENSP00000496036.1:p.Cys2034Tyr
|
|
ENST00000298820.7:c.1527+94G>A
|
|
|
ENST00000458043.6:c.6209G>A
|
ENSP00000400895.2:p.Cys2070Tyr
|
|
ENST00000546620.5:n.492G>A
|
|
|
ENST00000547103.5:c.6173G>A
|
ENSP00000447211.1:p.Cys2058Tyr
|
|
ENST00000550182.2:c.260G>A
|
ENSP00000449641.1:p.Cys87Tyr
|
|
ENST00000551340.5:c.364G>A
|
|
|
NM_173591.3:c.6209G>A
|
NP_775862.3:p.Cys2070Tyr
|
|
XM_005268802.2:c.6260G>A
|
XP_005268859.1:p.Cys2087Tyr
|
|
XM_011538191.1:c.6260G>A
|
XP_011536493.1:p.Cys2087Tyr
|
|
XM_011538192.1:c.6107G>A
|
XP_011536494.1:p.Cys2036Tyr
|
|
XM_011538193.1:c.5894G>A
|
XP_011536495.1:p.Cys1965Tyr
|
|
XM_005268802.3:c.6260G>A
|
XP_005268859.1:p.Cys2087Tyr
|
|
XM_011538192.2:c.6107G>A
|
XP_011536494.1:p.Cys2036Tyr
|
|
NM_001368062.1:c.6074G>A
|
NP_001354991.1:p.Cys2025Tyr
|
|
NM_001368062.3:c.6101G>A
|
NP_001354991.2:p.Cys2034Tyr
|
|
NM_001378609.3:c.6236G>A
MANE Select
|
NP_001365538.2:p.Cys2079Tyr
|
|
NM_001378610.3:c.6236G>A
|
NP_001365539.2:p.Cys2079Tyr
|
|
NM_173591.7:c.6236G>A
|
NP_775862.4:p.Cys2079Tyr
|
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