ENST00000376199.7:c.676G>T
|
ENSP00000365372.2:p.Ala226Ser
|
|
ENST00000376207.10:c.781G>T
MANE Select
|
ENSP00000365380.4:p.Ala261Ser
|
|
ENST00000455775.7:c.850G>T
|
ENSP00000396415.3:p.Ala284Ser
|
|
ENST00000518685.6:c.735+251G>T
|
ENSP00000428952.2:n.735+251G>T
|
|
ENST00000557224.6:c.676G>T
|
ENSP00000451208.1:p.Ala226Ser
|
|
ENST00000651307.1:c.781G>T
|
ENSP00000498454.1:p.Ala261Ser
|
|
ENST00000376197.1:c.631G>T
|
ENSP00000365369.1:p.Ala211Ser
|
|
ENST00000376199.6:c.676G>T
|
ENSP00000365372.2:p.Ala226Ser
|
|
ENST00000376207.8:c.781G>T
|
ENSP00000365380.4:p.Ala261Ser
|
|
ENST00000455775.6:c.850G>T
|
ENSP00000396415.3:p.Ala284Ser
|
|
ENST00000518685.5:c.676G>T
|
ENSP00000428952.1:p.Ala226Ser
|
|
ENST00000557224.5:c.676G>T
|
ENSP00000451208.1:p.Ala226Ser
|
|
NM_001114377.1:c.676G>T
|
NP_001107849.1:p.Ala226Ser
|
|
NM_014009.3:c.781G>T , LRG_62t1:c.781G>T
|
NP_054728.2:p.Ala261Ser
|
|
XM_006724533.2:c.850G>T
|
XP_006724596.2:p.Ala284Ser
|
|
XM_011543915.1:c.1000G>T
|
XP_011542217.1:p.Ala334Ser
|
|
XM_011543916.1:c.1000G>T
|
XP_011542218.1:p.Ala334Ser
|
|
XM_011543917.1:c.799G>T
|
XP_011542219.1:p.Ala267Ser
|
|
XM_011543918.1:c.1036G>T
|
XP_011542220.1:p.Ala346Ser
|
|
XM_011543919.1:c.1000G>T
|
XP_011542221.1:p.Ala334Ser
|
|
XM_017029567.1:c.727G>T
|
XP_016885056.1:p.Ala243Ser
|
|
NM_001114377.2:c.676G>T
|
NP_001107849.1:p.Ala226Ser
|
|
NM_014009.4:c.781G>T
MANE Select
|
NP_054728.2:p.Ala261Ser
|
|