ENST00000427262.6:c.585A=
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ENSP00000405052.1:p.Ala195=
|
|
ENST00000642232.1:c.765A=
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ENSP00000494064.1:p.Ala255=
|
|
ENST00000643230.2:c.765A=
MANE Select
|
ENSP00000496491.1:p.Ala255=
|
|
ENST00000643441.1:n.750A=
|
|
|
ENST00000644381.1:n.328A=
|
|
|
ENST00000307792.7:c.765A=
|
ENSP00000303212.3:p.Ala255=
|
|
ENST00000427262.5:c.585A=
|
ENSP00000405052.1:p.Ala195=
|
|
NM_001178129.1:c.585A=
|
NP_001171600.1:p.Ala195=
|
|
NM_012431.2:c.765A=
|
NP_036563.1:p.Ala255=
|
|
XM_011516715.1:c.765A=
|
XP_011515017.1:p.Ala255=
|
|
NM_012431.3:c.765A=
MANE Select
|
NP_036563.1:p.Ala255=
|
|
NM_001178129.2:c.585A=
|
NP_001171600.1:p.Ala195=
|
|