ENST00000347132.10:c.1517C>T
MANE Select
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ENSP00000262916.6:p.Ala506Val
|
|
ENST00000347132.9:c.1517C>T
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ENSP00000262916.6:p.Ala506Val
|
|
ENST00000443478.3:c.1098C>T
|
|
|
ENST00000506017.1:n.836C>T
|
|
|
ENST00000509682.6:c.1355C>T
|
ENSP00000423756.2:p.Ala452Val
|
|
NM_004700.3:c.1517C>T
|
NP_004691.2:p.Ala506Val
|
|
NM_172163.2:c.1355C>T
|
NP_751895.1:p.Ala452Val
|
|
XR_946798.1:n.1523C>T
|
|
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XR_946799.1:n.1523C>T
|
|
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XR_946800.1:n.1272C>T
|
|
|
XM_017002792.1:c.500C>T
|
XP_016858281.1:p.Ala167Val
|
|
NM_004700.4:c.1517C>T
MANE Select
|
NP_004691.2:p.Ala506Val
|
|
NM_172163.3:c.1355C>T
|
NP_751895.1:p.Ala452Val
|
|