ENST00000422447.8:c.871G>T
MANE Select
|
ENSP00000395337.3:p.Val291Phe
|
|
ENST00000227157.8:c.*21G>T
|
ENSP00000227157.4:n.*21G>T
|
|
ENST00000375710.7:n.1738G>T
|
|
|
ENST00000379412.9:c.871G>T
|
ENSP00000368722.5:p.Val291Phe
|
|
ENST00000396222.6:c.688-86G>T
|
ENSP00000379524.2:n.688-86G>T
|
|
ENST00000422447.7:c.871G>T
|
ENSP00000395337.3:p.Val291Phe
|
|
ENST00000430553.6:c.697G>T
|
ENSP00000406172.2:p.Val233Phe
|
|
ENST00000538451.1:n.758G>T
|
|
|
ENST00000540430.5:c.958G>T
|
ENSP00000445175.1:p.Val320Phe
|
|
ENST00000541097.5:c.*209G>T
|
ENSP00000443362.1:n.*209G>T
|
|
ENST00000542179.1:c.871G>T
|
ENSP00000445331.1:p.Val291Phe
|
|
ENST00000545215.5:c.*615G>T
|
ENSP00000442637.1:n.*615G>T
|
|
NM_001135239.1:c.697G>T
|
NP_001128711.1:p.Val233Phe
|
|
NM_001165414.1:c.958G>T
|
NP_001158886.1:p.Val320Phe
|
|
NM_001165415.1:c.688-86G>T
|
NP_001158887.1:n.688-86G>T
|
|
NM_001165416.1:c.*21G>T
|
NP_001158888.1:n.*21G>T
|
|
NM_005566.3:c.871G>T
|
NP_005557.1:p.Val291Phe
|
|
NR_028500.1:n.1025G>T
|
|
|
NM_005566.4:c.871G>T
MANE Select
|
NP_005557.1:p.Val291Phe
|
|
NM_001165415.2:c.688-86G>T
|
NP_001158887.1:n.688-86G>T
|
|
NM_001135239.2:c.697G>T
|
NP_001128711.1:p.Val233Phe
|
|
NM_001165414.2:c.958G>T
|
NP_001158886.1:p.Val320Phe
|
|
NM_001165416.2:c.*21G>T
|
NP_001158888.1:n.*21G>T
|
|
NR_028500.2:n.851G>T
|
|
|