ENST00000376199.7:c.959A>T
|
ENSP00000365372.2:p.Glu320Val
|
|
ENST00000376207.10:c.1064A>T
MANE Select
|
ENSP00000365380.4:p.Glu355Val
|
|
ENST00000455775.7:c.1133A>T
|
ENSP00000396415.3:p.Glu378Val
|
|
ENST00000518685.6:c.983A>T
|
ENSP00000428952.2:p.Glu328Val
|
|
ENST00000557224.6:c.959A>T
|
ENSP00000451208.1:p.Glu320Val
|
|
ENST00000651307.1:c.987A>T
|
ENSP00000498454.1:p.Arg329Ser
|
|
ENST00000376197.1:c.914A>T
|
ENSP00000365369.1:p.Glu305Val
|
|
ENST00000376199.6:c.959A>T
|
ENSP00000365372.2:p.Glu320Val
|
|
ENST00000376207.8:c.1064A>T
|
ENSP00000365380.4:p.Glu355Val
|
|
ENST00000455775.6:c.1133A>T
|
ENSP00000396415.3:p.Glu378Val
|
|
ENST00000518685.5:c.959A>T
|
ENSP00000428952.1:p.Glu320Val
|
|
ENST00000557224.5:c.959A>T
|
ENSP00000451208.1:p.Glu320Val
|
|
NM_001114377.1:c.959A>T
|
NP_001107849.1:p.Glu320Val
|
|
NM_014009.3:c.1064A>T , LRG_62t1:c.1064A>T
|
NP_054728.2:p.Glu355Val
|
|
XM_006724533.2:c.1133A>T
|
XP_006724596.2:p.Glu378Val
|
|
XM_011543915.1:c.1283A>T
|
XP_011542217.1:p.Glu428Val
|
|
XM_011543916.1:c.1283A>T
|
XP_011542218.1:p.Glu428Val
|
|
XM_011543917.1:c.1082A>T
|
XP_011542219.1:p.Glu361Val
|
|
XM_011543918.1:c.1319A>T
|
XP_011542220.1:p.Glu440Val
|
|
XM_011543919.1:c.1283A>T
|
XP_011542221.1:p.Glu428Val
|
|
XM_017029567.1:c.1010A>T
|
XP_016885056.1:p.Glu337Val
|
|
NM_001114377.2:c.959A>T
|
NP_001107849.1:p.Glu320Val
|
|
NM_014009.4:c.1064A>T
MANE Select
|
NP_054728.2:p.Glu355Val
|
|