ENST00000426263.10:c.39G>T
MANE Select
|
ENSP00000416293.2:p.Met13Ile
|
|
ENST00000674765.1:c.39G>T
|
ENSP00000501811.1:p.Met13Ile
|
|
ENST00000675112.1:n.62G>T
|
|
|
ENST00000372500.4:c.19-12095G>T
|
ENSP00000361578.4:n.19-12095G>T
|
|
ENST00000415851.6:n.256G>T
|
|
|
ENST00000426263.7:c.39G>T
|
ENSP00000416293.2:p.Met13Ile
|
|
ENST00000625233.2:n.247G>T
|
|
|
ENST00000628173.1:n.258G>T
|
|
|
ENST00000630287.2:c.39G>T
|
ENSP00000486694.1:p.Met13Ile
|
|
ENST00000630821.1:n.256G>T
|
|
|
NM_006516.2:c.39G>T
|
NP_006507.2:p.Met13Ile
|
|
NM_006516.3:c.39G>T
|
NP_006507.2:p.Met13Ile
|
|
NM_006516.4:c.39G>T
MANE Select
|
NP_006507.2:p.Met13Ile
|
|