|
NM_006736.6:c.645C>T
MANE Select
|
NP_006727.2:p.Gly215=
|
|
ENST00000336576.10:c.645C>T
MANE Select
|
ENSP00000338019.5:p.Gly215=
|
|
NM_001039550.1:c.645C>T
|
NP_001034639.1:p.Gly215=
|
|
NM_001039550.2:c.645C>T
|
NP_001034639.1:p.Gly215=
|
|
NM_006736.5:c.645C>T
|
NP_006727.2:p.Gly215=
|
|
ENST00000336576.9:c.645C>T
|
ENSP00000338019.5:p.Gly215=
|
|
ENST00000392086.8:c.645C>T
|
ENSP00000375936.4:p.Gly215=
|
|
ENST00000392087.6:c.552C>T
|
ENSP00000375937.2:p.Gly184=
|
|
ENST00000425450.5:c.645C>T
|
ENSP00000414796.1:p.Gly215=
|
|
ENST00000463463.5:n.636C>T
|
|
|
ENST00000472019.5:n.388C>T
|
|
|
ENST00000473750.5:n.432C>T
|
|
|
ENST00000476254.1:n.269C>T
|
|
|
ENST00000477917.5:n.2249C>T
|
|
|
ENST00000684599.1:n.852C>T
|
|