ENST00000597921.6:c.534C>T
MANE Select
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ENSP00000471974.1:p.Gly178=
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ENST00000346664.9:c.534C>T
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ENSP00000264072.6:p.Gly178=
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|
ENST00000360067.8:c.531C>T
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ENSP00000353178.4:p.Gly177=
|
|
ENST00000593418.1:c.471C>T
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ENSP00000472067.1:p.Gly157=
|
|
ENST00000597312.5:n.1059C>T
|
|
|
ENST00000597921.5:c.534C>T
|
ENSP00000471974.1:p.Gly178=
|
|
ENST00000597934.1:n.896C>T
|
|
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ENST00000598803.5:n.1029C>T
|
|
|
NM_001207019.2:c.531C>T
|
NP_001193948.2:p.Gly177=
|
|
NM_001220500.1:c.534C>T
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NP_001207429.1:p.Gly178=
|
|
NM_002002.4:c.534C>T
|
NP_001993.2:p.Gly178=
|
|
XM_005272462.3:c.534C>T
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XP_005272519.1:p.Gly178=
|
|
XM_005272462.4:c.534C>T
|
XP_005272519.1:p.Gly178=
|
|
NM_001220500.2:c.534C>T
MANE Select
|
NP_001207429.1:p.Gly178=
|
|
NM_001207019.3:c.531C>T
|
NP_001193948.2:p.Gly177=
|
|
NM_002002.5:c.534C>T
|
NP_001993.2:p.Gly178=
|
|