ENST00000525341.2:c.1196G>T
|
|
|
ENST00000528641.7:c.700G>T
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ENSP00000434982.3:p.Ala234Ser
|
|
ENST00000529797.2:n.1731G>T
|
|
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ENST00000682324.1:c.469-108G>T
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ENSP00000508017.1:n.469-108G>T
|
|
ENST00000682659.1:c.520G>T
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ENSP00000507351.1:p.Ala174Ser
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ENST00000682699.1:c.889G>T
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ENSP00000507935.1:p.Ala297Ser
|
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ENST00000683237.1:c.*29G>T
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ENSP00000507343.1:n.*29G>T
|
|
ENST00000683856.1:c.712G>T
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ENSP00000507979.1:p.Ala238Ser
|
|
ENST00000684006.1:c.*29G>T
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ENSP00000507269.1:n.*29G>T
|
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ENST00000684657.1:c.709G>T
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ENSP00000507961.1:p.Ala237Ser
|
|
ENST00000279146.8:c.889G>T
MANE Select
|
ENSP00000279146.3:p.Ala297Ser
|
|
ENST00000279146.7:c.889G>T
|
ENSP00000279146.3:p.Ala297Ser
|
|
NM_001302959.1:c.712G>T
|
NP_001289888.1:p.Ala238Ser
|
|
NM_001302960.1:c.*29G>T
|
NP_001289889.1:n.*29G>T
|
|
NM_003977.3:c.889G>T
|
NP_003968.3:p.Ala297Ser
|
|
XM_024448761.1:c.889G>T
|
XP_024304529.1:p.Ala297Ser
|
|
NM_003977.4:c.889G>T
MANE Select
|
NP_003968.3:p.Ala297Ser
|
|
NM_001302960.2:c.*29G>T
|
NP_001289889.1:n.*29G>T
|
|
NM_001302959.2:c.712G>T
|
NP_001289888.1:p.Ala238Ser
|
|