ENST00000331433.5:c.299C>A
MANE Select
|
ENSP00000332771.4:p.Pro100His
|
|
ENST00000331433.4:c.299C>A
|
ENSP00000332771.4:p.Pro100His
|
|
ENST00000375692.5:c.299C>A
|
ENSP00000364844.1:p.Pro100His
|
|
ENST00000439316.6:c.229+904C>A
|
ENSP00000414445.2:n.229+904C>A
|
|
ENST00000464764.5:n.889-27C>A
|
|
|
ENST00000495784.1:n.457C>A
|
|
|
NM_001042704.1:c.299C>A
|
NP_001036169.1:p.Pro100His
|
|
NM_001257139.1:c.229+904C>A
|
NP_001244068.1:n.229+904C>A
|
|
NM_004070.3:c.299C>A
|
NP_004061.3:p.Pro100His
|
|
NM_004070.4:c.299C>A
MANE Select
|
NP_004061.3:p.Pro100His
|
|
NM_001042704.2:c.299C>A
|
NP_001036169.1:p.Pro100His
|
|
NM_001257139.2:c.229+904C>A
|
NP_001244068.1:n.229+904C>A
|
|