ENST00000256906.5:c.528C>T
MANE Select
|
ENSP00000256906.4:p.Ala176=
|
|
ENST00000256906.4:c.528C>T
|
ENSP00000256906.4:p.Ala176=
|
|
ENST00000426880.2:c.264C>T
|
ENSP00000402526.2:p.Ala88=
|
|
NM_001143828.1:c.264C>T
|
NP_001137300.1:p.Ala88=
|
|
NM_001160166.1:c.*160C>T
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NP_001153638.1:n.*160C>T
|
|
NM_021624.3:c.528C>T
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NP_067637.2:p.Ala176=
|
|
XM_011526133.1:c.357+7966C>T
|
XP_011524435.1:n.357+7966C>T
|
|
NM_021624.4:c.528C>T
MANE Select
|
NP_067637.2:p.Ala176=
|
|
NM_001143828.2:c.264C>T
|
NP_001137300.1:p.Ala88=
|
|
NM_001160166.2:c.*160C>T
|
NP_001153638.1:n.*160C>T
|
|