ENST00000422447.8:c.994T>C
MANE Select
|
ENSP00000395337.3:p.Phe332Leu
|
|
ENST00000227157.8:c.*144T>C
|
ENSP00000227157.4:n.*144T>C
|
|
ENST00000375710.7:n.1861T>C
|
|
|
ENST00000379412.9:c.994T>C
|
ENSP00000368722.5:p.Phe332Leu
|
|
ENST00000396222.6:c.725T>C
|
ENSP00000379524.2:p.Ile242Thr
|
|
ENST00000422447.7:c.994T>C
|
ENSP00000395337.3:p.Phe332Leu
|
|
ENST00000430553.6:c.820T>C
|
ENSP00000406172.2:p.Phe274Leu
|
|
ENST00000538451.1:n.881T>C
|
|
|
ENST00000540430.5:c.1081T>C
|
ENSP00000445175.1:p.Phe361Leu
|
|
ENST00000542179.1:c.994T>C
|
ENSP00000445331.1:p.Phe332Leu
|
|
ENST00000545215.5:c.*738T>C
|
ENSP00000442637.1:n.*738T>C
|
|
NM_001135239.1:c.820T>C
|
NP_001128711.1:p.Phe274Leu
|
|
NM_001165414.1:c.1081T>C
|
NP_001158886.1:p.Phe361Leu
|
|
NM_001165415.1:c.725T>C
|
NP_001158887.1:p.Ile242Thr
|
|
NM_001165416.1:c.*144T>C
|
NP_001158888.1:n.*144T>C
|
|
NM_005566.3:c.994T>C
|
NP_005557.1:p.Phe332Leu
|
|
NR_028500.1:n.1148T>C
|
|
|
NM_005566.4:c.994T>C
MANE Select
|
NP_005557.1:p.Phe332Leu
|
|
NM_001165415.2:c.725T>C
|
NP_001158887.1:p.Ile242Thr
|
|
NM_001135239.2:c.820T>C
|
NP_001128711.1:p.Phe274Leu
|
|
NM_001165414.2:c.1081T>C
|
NP_001158886.1:p.Phe361Leu
|
|
NM_001165416.2:c.*144T>C
|
NP_001158888.1:n.*144T>C
|
|
NR_028500.2:n.974T>C
|
|
|