ENST00000383788.10:c.751C>T
MANE Select
|
ENSP00000373298.3:p.Pro251Ser
|
|
ENST00000604401.2:n.747C>T
|
|
|
ENST00000679838.1:c.*513C>T
|
ENSP00000505708.1:n.*513C>T
|
|
ENST00000680545.1:n.517C>T
|
|
|
ENST00000681097.1:c.751C>T
|
ENSP00000505397.1:p.Pro251Ser
|
|
ENST00000383781.8:c.721C>T
|
ENSP00000373291.3:p.Pro241Ser
|
|
ENST00000383786.9:c.649C>T
|
ENSP00000373296.3:p.Pro217Ser
|
|
ENST00000383788.9:c.751C>T
|
ENSP00000373298.3:p.Pro251Ser
|
|
ENST00000603808.5:c.751C>T
|
ENSP00000474271.1:p.Pro251Ser
|
|
ENST00000605797.1:c.580C>T
|
ENSP00000474936.1:p.Pro194Ser
|
|
NM_005677.3:c.751C>T
|
NP_005668.2:p.Pro251Ser
|
|
NM_080538.2:c.721C>T
|
NP_536799.1:p.Pro241Ser
|
|
NM_080539.3:c.649C>T
|
NP_536800.2:p.Pro217Ser
|
|
NM_005677.4:c.751C>T
MANE Select
|
NP_005668.2:p.Pro251Ser
|
|
NM_080539.4:c.649C>T
|
NP_536800.2:p.Pro217Ser
|
|