ENST00000376199.7:c.681G>T
|
ENSP00000365372.2:p.Gly227=
|
|
ENST00000376207.10:c.786G>T
MANE Select
|
ENSP00000365380.4:p.Gly262=
|
|
ENST00000455775.7:c.855G>T
|
ENSP00000396415.3:p.Gly285=
|
|
ENST00000518685.6:c.735+256G>T
|
ENSP00000428952.2:n.735+256G>T
|
|
ENST00000557224.6:c.681G>T
|
ENSP00000451208.1:p.Gly227=
|
|
ENST00000651307.1:c.786G>T
|
ENSP00000498454.1:p.Gly262=
|
|
ENST00000376197.1:c.636G>T
|
ENSP00000365369.1:p.Gly212=
|
|
ENST00000376199.6:c.681G>T
|
ENSP00000365372.2:p.Gly227=
|
|
ENST00000376207.8:c.786G>T
|
ENSP00000365380.4:p.Gly262=
|
|
ENST00000455775.6:c.855G>T
|
ENSP00000396415.3:p.Gly285=
|
|
ENST00000518685.5:c.681G>T
|
ENSP00000428952.1:p.Gly227=
|
|
ENST00000557224.5:c.681G>T
|
ENSP00000451208.1:p.Gly227=
|
|
NM_001114377.1:c.681G>T
|
NP_001107849.1:p.Gly227=
|
|
NM_014009.3:c.786G>T , LRG_62t1:c.786G>T
|
NP_054728.2:p.Gly262=
|
|
XM_006724533.2:c.855G>T
|
XP_006724596.2:p.Gly285=
|
|
XM_011543915.1:c.1005G>T
|
XP_011542217.1:p.Gly335=
|
|
XM_011543916.1:c.1005G>T
|
XP_011542218.1:p.Gly335=
|
|
XM_011543917.1:c.804G>T
|
XP_011542219.1:p.Gly268=
|
|
XM_011543918.1:c.1041G>T
|
XP_011542220.1:p.Gly347=
|
|
XM_011543919.1:c.1005G>T
|
XP_011542221.1:p.Gly335=
|
|
XM_017029567.1:c.732G>T
|
XP_016885056.1:p.Gly244=
|
|
NM_001114377.2:c.681G>T
|
NP_001107849.1:p.Gly227=
|
|
NM_014009.4:c.786G>T
MANE Select
|
NP_054728.2:p.Gly262=
|
|