ENST00000231420.11:c.1507T=
MANE Select
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ENSP00000231420.6:p.Ser503=
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ENST00000231420.10:c.1507T=
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ENSP00000231420.6:p.Ser503=
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|
ENST00000510428.1:c.1282T=
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ENSP00000422799.1:p.Ser428=
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|
ENST00000512135.5:n.1177T=
|
|
|
ENST00000618015.4:c.1282T=
|
ENSP00000479154.1:p.Ser428=
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|
NM_001306173.1:c.1282T=
|
NP_001293102.1:p.Ser428=
|
|
NM_031900.3:c.1507T=
|
NP_114106.1:p.Ser503=
|
|
XM_005248337.2:c.1504T=
|
XP_005248394.1:p.Ser502=
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|
XM_005248338.2:c.1312T=
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XP_005248395.1:p.Ser438=
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|
XM_011514077.1:c.1438-355T=
|
XP_011512379.1:n.1438-355T=
|
|
XM_005248337.3:c.1504T=
|
XP_005248394.1:p.Ser502=
|
|
XM_005248338.3:c.1312T=
|
XP_005248395.1:p.Ser438=
|
|
XM_017009748.2:c.1282T=
|
XP_016865237.1:p.Ser428=
|
|
NM_031900.4:c.1507T=
MANE Select
|
NP_114106.1:p.Ser503=
|
|
NM_001306173.2:c.1282T=
|
NP_001293102.1:p.Ser428=
|
|