ENST00000376199.7:c.700G>T
|
ENSP00000365372.2:p.Ala234Ser
|
|
ENST00000376207.10:c.805G>T
MANE Select
|
ENSP00000365380.4:p.Ala269Ser
|
|
ENST00000455775.7:c.874G>T
|
ENSP00000396415.3:p.Ala292Ser
|
|
ENST00000518685.6:c.735+275G>T
|
ENSP00000428952.2:n.735+275G>T
|
|
ENST00000557224.6:c.700G>T
|
ENSP00000451208.1:p.Ala234Ser
|
|
ENST00000651307.1:c.805G>T
|
ENSP00000498454.1:p.Ala269Ser
|
|
ENST00000376197.1:c.655G>T
|
ENSP00000365369.1:p.Ala219Ser
|
|
ENST00000376199.6:c.700G>T
|
ENSP00000365372.2:p.Ala234Ser
|
|
ENST00000376207.8:c.805G>T
|
ENSP00000365380.4:p.Ala269Ser
|
|
ENST00000455775.6:c.874G>T
|
ENSP00000396415.3:p.Ala292Ser
|
|
ENST00000518685.5:c.700G>T
|
ENSP00000428952.1:p.Ala234Ser
|
|
ENST00000557224.5:c.700G>T
|
ENSP00000451208.1:p.Ala234Ser
|
|
NM_001114377.1:c.700G>T
|
NP_001107849.1:p.Ala234Ser
|
|
NM_014009.3:c.805G>T , LRG_62t1:c.805G>T
|
NP_054728.2:p.Ala269Ser
|
|
XM_006724533.2:c.874G>T
|
XP_006724596.2:p.Ala292Ser
|
|
XM_011543915.1:c.1024G>T
|
XP_011542217.1:p.Ala342Ser
|
|
XM_011543916.1:c.1024G>T
|
XP_011542218.1:p.Ala342Ser
|
|
XM_011543917.1:c.823G>T
|
XP_011542219.1:p.Ala275Ser
|
|
XM_011543918.1:c.1060G>T
|
XP_011542220.1:p.Ala354Ser
|
|
XM_011543919.1:c.1024G>T
|
XP_011542221.1:p.Ala342Ser
|
|
XM_017029567.1:c.751G>T
|
XP_016885056.1:p.Ala251Ser
|
|
NM_001114377.2:c.700G>T
|
NP_001107849.1:p.Ala234Ser
|
|
NM_014009.4:c.805G>T
MANE Select
|
NP_054728.2:p.Ala269Ser
|
|