ENST00000295897.9:c.1088C>A
MANE Select
|
ENSP00000295897.4:p.Pro363His
|
|
ENST00000295897.8:c.1088C>A
|
ENSP00000295897.4:p.Pro363His
|
|
ENST00000401494.7:c.743C>A
|
ENSP00000384695.3:p.Pro248His
|
|
ENST00000415165.6:c.512C>A
|
ENSP00000401820.2:p.Pro171His
|
|
ENST00000476441.6:c.*367C>A
|
ENSP00000423727.1:n.*367C>A
|
|
ENST00000484992.1:n.408C>A
|
|
|
ENST00000503124.5:c.638C>A
|
ENSP00000421027.1:p.Pro213His
|
|
ENST00000504043.1:n.91C>A
|
|
|
ENST00000505649.5:n.774C>A
|
|
|
ENST00000509063.5:c.1088C>A
|
ENSP00000422784.1:p.Pro363His
|
|
ENST00000511370.1:c.621C>A
|
|
|
ENST00000621085.4:c.491-42C>A
|
ENSP00000483421.1:n.491-42C>A
|
|
ENST00000621628.4:c.487-38C>A
|
ENSP00000480485.1:n.487-38C>A
|
|
NM_000477.5:c.1088C>A
|
NP_000468.1:p.Pro363His
|
|
NM_000477.6:c.1088C>A
|
NP_000468.1:p.Pro363His
|
|
NM_000477.7:c.1088C>A
MANE Select
|
NP_000468.1:p.Pro363His
|
|