ENST00000295897.9:c.1157C>T
MANE Select
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ENSP00000295897.4:p.Ala386Val
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ENST00000295897.8:c.1157C>T
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ENSP00000295897.4:p.Ala386Val
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|
ENST00000401494.7:c.812C>T
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ENSP00000384695.3:p.Ala271Val
|
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ENST00000415165.6:c.581C>T
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ENSP00000401820.2:p.Ala194Val
|
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ENST00000476441.6:c.*436C>T
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ENSP00000423727.1:n.*436C>T
|
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ENST00000484992.1:n.477C>T
|
|
|
ENST00000503124.5:c.707C>T
|
ENSP00000421027.1:p.Ala236Val
|
|
ENST00000504043.1:n.160C>T
|
|
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ENST00000505649.5:n.843C>T
|
|
|
ENST00000509063.5:c.1157C>T
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ENSP00000422784.1:p.Ala386Val
|
|
ENST00000511370.1:c.690C>T
|
|
|
ENST00000621085.4:c.518C>T
|
ENSP00000483421.1:p.Ala173Val
|
|
ENST00000621628.4:c.518C>T
|
ENSP00000480485.1:p.Ala173Val
|
|
NM_000477.5:c.1157C>T
|
NP_000468.1:p.Ala386Val
|
|
NM_000477.6:c.1157C>T
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NP_000468.1:p.Ala386Val
|
|
NM_000477.7:c.1157C>T
MANE Select
|
NP_000468.1:p.Ala386Val
|
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