ENST00000647165.2:c.7231G>T
MANE Select
|
ENSP00000495481.1:p.Ala2411Ser
|
|
ENST00000205890.9:c.7231G>T
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ENSP00000205890.5:p.Ala2411Ser
|
|
ENST00000615845.4:c.7231G>T
|
ENSP00000481642.1:p.Ala2411Ser
|
|
NM_016239.3:c.7231G>T
|
NP_057323.3:p.Ala2411Ser
|
|
XM_011523917.1:c.6906G>T
|
XP_011522219.1:p.Gln2302His
|
|
XM_011523921.1:c.7225G>T
|
XP_011522223.1:p.Ala2409Ser
|
|
XR_934037.1:n.7565G>T
|
|
|
XR_934038.1:n.7517G>T
|
|
|
XR_934293.1:n.434+1156C>A
|
|
|
XR_934294.1:n.435-674C>A
|
|
|
XR_934295.1:n.253+1156C>A
|
|
|
XM_017024714.2:c.7171G>T
|
XP_016880203.1:p.Ala2391Ser
|
|
XM_017024715.2:c.7234G>T
|
XP_016880204.1:p.Ala2412Ser
|
|
XR_934293.2:n.377+1156C>A
|
|
|
XR_934294.2:n.378-674C>A
|
|
|
NM_016239.4:c.7231G>T
MANE Select
|
NP_057323.3:p.Ala2411Ser
|
|