ENST00000309755.9:c.1454T>C
MANE Select
|
ENSP00000312397.4:p.Val485Ala
|
|
ENST00000309755.8:c.1454T>C
|
ENSP00000312397.4:p.Val485Ala
|
|
ENST00000447439.6:n.1510T>C
|
|
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ENST00000504208.5:c.*338T>C
|
ENSP00000423585.1:n.*338T>C
|
|
ENST00000506491.5:c.1208T>C
|
ENSP00000424828.1:p.Val403Ala
|
|
ENST00000506873.5:n.977T>C
|
|
|
ENST00000508657.5:c.1358T>C
|
ENSP00000422099.1:p.Val453Ala
|
|
ENST00000509694.1:n.247T>C
|
|
|
NM_001257194.1:c.1358T>C
|
NP_001244123.1:p.Val453Ala
|
|
NM_001257195.1:c.1208T>C
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NP_001244124.1:p.Val403Ala
|
|
NM_017415.2:c.1454T>C
|
NP_059111.2:p.Val485Ala
|
|
NM_017415.3:c.1454T>C
MANE Select
|
NP_059111.2:p.Val485Ala
|
|
NM_001257195.2:c.1208T>C
|
NP_001244124.1:p.Val403Ala
|
|