|
ENST00000327956.7:c.3078A=
|
ENSP00000333674.7:p.Thr1026=
|
|
|
ENST00000333535.9:c.3078A=
|
ENSP00000328968.4:p.Thr1026=
|
|
|
ENST00000413689.6:c.3078A=
MANE Plus Clinical
|
ENSP00000410257.1:p.Thr1026=
|
|
|
ENST00000423572.7:c.3078A=
MANE Select
|
ENSP00000398266.2:p.Thr1026=
|
|
|
ENST00000333535.8:c.3078A=
|
ENSP00000328968.4:p.Thr1026=
|
|
|
ENST00000413689.5:c.3078A=
|
ENSP00000410257.1:p.Thr1026=
|
|
|
ENST00000414099.6:c.3078A=
|
ENSP00000398962.2:p.Thr1026=
|
|
|
ENST00000423572.6:c.3078A=
|
ENSP00000398266.2:p.Thr1026=
|
|
|
ENST00000425664.5:c.3078A=
|
ENSP00000416634.1:p.Thr1026=
|
|
|
ENST00000449557.6:c.3078A=
|
ENSP00000413996.2:p.Thr1026=
|
|
|
ENST00000450102.6:c.3078A=
|
ENSP00000403355.2:p.Thr1026=
|
|
|
ENST00000451551.6:c.3078A=
|
ENSP00000388797.2:p.Thr1026=
|
|
|
ENST00000455624.6:c.3078A=
|
ENSP00000399524.2:p.Thr1026=
|
|
|
NM_000335.4:c.3078A= , LRG_289t2:c.3078A=
|
NP_000326.2:p.Thr1026=
|
|
|
NM_001099404.1:c.3078A= , LRG_289t3:c.3078A=
|
NP_001092874.1:p.Thr1026=
|
|
|
NM_001099405.1:c.3078A=
|
NP_001092875.1:p.Thr1026=
|
|
|
NM_001160160.1:c.3078A=
|
NP_001153632.1:p.Thr1026=
|
|
|
NM_001160161.1:c.3078A=
|
NP_001153633.1:p.Thr1026=
|
|
|
NM_198056.2:c.3078A= , LRG_289t1:c.3078A=
|
NP_932173.1:p.Thr1026=
|
|
|
XM_006713282.2:c.3078A=
|
XP_006713345.1:p.Thr1026=
|
|
|
XM_011533991.1:c.3078A=
|
XP_011532293.1:p.Thr1026=
|
|
|
XM_011533992.1:c.2949A=
|
XP_011532294.1:p.Thr983=
|
|
|
NM_001354701.1:c.3078A=
|
NP_001341630.1:p.Thr1026=
|
|
|
XM_011533991.2:c.3078A=
|
XP_011532293.1:p.Thr1026=
|
|
|
XM_017007017.1:c.3078A=
|
XP_016862506.1:p.Thr1026=
|
|
|
NM_000335.5:c.3078A=
MANE Select
|
NP_000326.2:p.Thr1026=
|
|
|
NM_001160160.2:c.3078A=
|
NP_001153632.1:p.Thr1026=
|
|
|
NM_001354701.2:c.3078A=
|
NP_001341630.1:p.Thr1026=
|
|
|
NM_001099404.2:c.3078A=
MANE Plus Clinical
|
NP_001092874.1:p.Thr1026=
|
|
|
NM_001099405.2:c.3078A=
|
NP_001092875.1:p.Thr1026=
|
|
|
NM_001160161.2:c.3078A=
|
NP_001153633.1:p.Thr1026=
|
|
|
NM_198056.3:c.3078A=
|
NP_932173.1:p.Thr1026=
|
|
