ENST00000426263.10:c.814A>G
MANE Select
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ENSP00000416293.2:p.Ile272Val
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|
ENST00000669445.1:c.144A>G
|
|
|
ENST00000674765.1:c.814A>G
|
ENSP00000501811.1:p.Ile272Val
|
|
ENST00000675112.1:n.837A>G
|
|
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ENST00000676254.1:n.1263A>G
|
|
|
ENST00000426263.7:c.814A>G
|
ENSP00000416293.2:p.Ile272Val
|
|
ENST00000439722.2:c.693A>G
|
ENSP00000395521.2:n.693A>G
|
|
ENST00000475162.3:c.415+980A>G
|
|
|
ENST00000630287.2:c.*129A>G
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ENSP00000486694.1:n.*129A>G
|
|
NM_006516.2:c.814A>G
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NP_006507.2:p.Ile272Val
|
|
NM_006516.3:c.814A>G
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NP_006507.2:p.Ile272Val
|
|
NM_006516.4:c.814A>G
MANE Select
|
NP_006507.2:p.Ile272Val
|
|