ENST00000302746.11:c.441C>A
MANE Select
|
ENSP00000307241.6:p.Pro147=
|
|
ENST00000302746.10:c.441C>A
|
ENSP00000307241.6:p.Pro147=
|
|
ENST00000383714.8:c.387C>A
|
ENSP00000373220.4:p.Pro129=
|
|
ENST00000461692.5:n.554C>A
|
|
|
ENST00000469364.5:c.441C>A
|
ENSP00000419580.1:p.Pro147=
|
|
ENST00000474765.1:c.387C>A
|
ENSP00000418448.1:p.Pro129=
|
|
ENST00000479945.1:n.2846C>A
|
|
|
ENST00000480626.5:n.533C>A
|
|
|
ENST00000485460.5:c.404-17C>A
|
ENSP00000417267.1:n.404-17C>A
|
|
NM_000925.3:c.441C>A
|
NP_000916.2:p.Pro147=
|
|
NM_001173468.1:c.404-17C>A
|
NP_001166939.1:n.404-17C>A
|
|
NM_001315536.1:c.387C>A
|
NP_001302465.1:p.Pro129=
|
|
NR_033384.1:n.554C>A
|
|
|
NM_000925.4:c.441C>A
MANE Select
|
NP_000916.2:p.Pro147=
|
|
NM_001173468.2:c.404-17C>A
|
NP_001166939.1:n.404-17C>A
|
|
NM_001315536.2:c.387C>A
|
NP_001302465.1:p.Pro129=
|
|
NR_033384.2:n.547C>A
|
|
|