ENST00000525341.2:c.1172G>T
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ENST00000528641.7:c.676G>T
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ENSP00000434982.3:p.Ala226Ser
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ENST00000529797.2:n.1707G>T
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ENST00000682324.1:c.469-132G>T
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ENSP00000508017.1:n.469-132G>T
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ENST00000682659.1:c.496G>T
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ENSP00000507351.1:p.Ala166Ser
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ENST00000682699.1:c.865G>T
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ENSP00000507935.1:p.Ala289Ser
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ENST00000683237.1:c.*5G>T
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ENSP00000507343.1:n.*5G>T
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ENST00000683856.1:c.688G>T
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ENSP00000507979.1:p.Ala230Ser
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ENST00000684006.1:c.*5G>T
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ENSP00000507269.1:n.*5G>T
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ENST00000684657.1:c.685G>T
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ENSP00000507961.1:p.Ala229Ser
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ENST00000279146.8:c.865G>T
MANE Select
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ENSP00000279146.3:p.Ala289Ser
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ENST00000279146.7:c.865G>T
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ENSP00000279146.3:p.Ala289Ser
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ENST00000528641.6:c.676G>T
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ENSP00000434982.2:p.Ala226Ser
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NM_001302959.1:c.688G>T
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NP_001289888.1:p.Ala230Ser
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NM_001302960.1:c.*5G>T
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NP_001289889.1:n.*5G>T
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NM_003977.3:c.865G>T
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NP_003968.3:p.Ala289Ser
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XM_024448761.1:c.865G>T
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XP_024304529.1:p.Ala289Ser
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NM_003977.4:c.865G>T
MANE Select
|
NP_003968.3:p.Ala289Ser
|
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NM_001302960.2:c.*5G>T
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NP_001289889.1:n.*5G>T
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NM_001302959.2:c.688G>T
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NP_001289888.1:p.Ala230Ser
|
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