ENST00000525341.2:c.740T>G
|
|
|
ENST00000528641.7:c.574T>G
|
ENSP00000434982.3:p.Ser192Ala
|
|
ENST00000529797.2:n.1275T>G
|
|
|
ENST00000682324.1:c.469-564T>G
|
ENSP00000508017.1:n.469-564T>G
|
|
ENST00000682659.1:c.394T>G
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ENSP00000507351.1:p.Ser132Ala
|
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ENST00000682699.1:c.763T>G
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ENSP00000507935.1:p.Ser255Ala
|
|
ENST00000683237.1:c.763T>G
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ENSP00000507343.1:p.Ser255Ala
|
|
ENST00000683856.1:c.586T>G
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ENSP00000507979.1:p.Ser196Ala
|
|
ENST00000684006.1:c.763T>G
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ENSP00000507269.1:p.Ser255Ala
|
|
ENST00000684657.1:c.583T>G
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ENSP00000507961.1:p.Ser195Ala
|
|
ENST00000279146.8:c.763T>G
MANE Select
|
ENSP00000279146.3:p.Ser255Ala
|
|
ENST00000279146.7:c.763T>G
|
ENSP00000279146.3:p.Ser255Ala
|
|
ENST00000525341.1:c.415T>G
|
ENSP00000476993.1:p.Ser139Ala
|
|
ENST00000528641.6:c.574T>G
|
ENSP00000434982.2:p.Ser192Ala
|
|
NM_001302959.1:c.586T>G
|
NP_001289888.1:p.Ser196Ala
|
|
NM_001302960.1:c.763T>G
|
NP_001289889.1:p.Ser255Ala
|
|
NM_003977.3:c.763T>G
|
NP_003968.3:p.Ser255Ala
|
|
XM_024448761.1:c.763T>G
|
XP_024304529.1:p.Ser255Ala
|
|
NM_003977.4:c.763T>G
MANE Select
|
NP_003968.3:p.Ser255Ala
|
|
NM_001302960.2:c.763T>G
|
NP_001289889.1:p.Ser255Ala
|
|
NM_001302959.2:c.586T>G
|
NP_001289888.1:p.Ser196Ala
|
|