ENST00000427724.7:c.3648C>T
|
ENSP00000390717.3:p.Gly1216=
|
|
ENST00000643257.2:c.3765C>T
MANE Select
|
ENSP00000493815.1:p.Gly1255=
|
|
ENST00000650162.1:c.3420C>T
|
ENSP00000497075.1:p.Gly1140=
|
|
ENST00000674413.1:c.3164C>T
|
|
|
ENST00000323668.11:c.3531C>T
|
ENSP00000325223.6:p.Gly1177=
|
|
ENST00000377797.7:c.3762C>T
|
ENSP00000367028.4:p.Gly1254=
|
|
ENST00000427724.6:c.3648C>T
|
ENSP00000390717.2:p.Gly1216=
|
|
ENST00000439160.6:c.3651C>T
|
ENSP00000406888.2:p.Gly1217=
|
|
ENST00000445265.6:c.3534C>T
|
ENSP00000409944.2:p.Gly1178=
|
|
ENST00000504761.6:c.3762C>T
|
ENSP00000421655.2:p.Gly1254=
|
|
ENST00000513346.5:c.3762C>T
|
ENSP00000427484.1:p.Gly1254=
|
|
ENST00000514442.5:n.3812C>T
|
|
|
ENST00000515516.1:c.343-3210C>T
|
ENSP00000426471.1:n.343-3210C>T
|
|
NM_000356.3:c.3531C>T
|
NP_000347.2:p.Gly1177=
|
|
NM_001135243.1:c.3762C>T
|
NP_001128715.1:p.Gly1254=
|
|
NM_001135244.1:c.3651C>T
|
NP_001128716.1:p.Gly1217=
|
|
NM_001135245.1:c.3534C>T
|
NP_001128717.1:p.Gly1178=
|
|
NM_001195141.1:c.3648C>T
|
NP_001182070.1:p.Gly1216=
|
|
XM_005268502.2:c.3876C>T
|
XP_005268559.1:p.Gly1292=
|
|
XM_005268503.2:c.3873C>T
|
XP_005268560.1:p.Gly1291=
|
|
XM_005268504.2:c.3873C>T
|
XP_005268561.1:p.Gly1291=
|
|
XM_005268505.2:c.3765C>T
|
XP_005268562.1:p.Gly1255=
|
|
XM_005268506.2:c.3762C>T
|
XP_005268563.1:p.Gly1254=
|
|
XM_005268507.2:c.3645C>T
|
XP_005268564.1:p.Gly1215=
|
|
XM_011537678.1:c.3696C>T
|
XP_011535980.1:p.Gly1232=
|
|
XM_005268502.4:c.3876C>T
|
XP_005268559.1:p.Gly1292=
|
|
XM_005268503.4:c.3873C>T
|
XP_005268560.1:p.Gly1291=
|
|
XM_005268504.4:c.3873C>T
|
XP_005268561.1:p.Gly1291=
|
|
XM_005268505.4:c.3765C>T
|
XP_005268562.1:p.Gly1255=
|
|
XM_005268506.4:c.3762C>T
|
XP_005268563.1:p.Gly1254=
|
|
XM_005268507.4:c.3645C>T
|
XP_005268564.1:p.Gly1215=
|
|
XM_011537678.3:c.3696C>T
|
XP_011535980.1:p.Gly1232=
|
|
XM_017009792.2:c.3759C>T
|
XP_016865281.1:p.Gly1253=
|
|
XM_017009793.2:c.3585C>T
|
XP_016865282.1:p.Gly1195=
|
|
XM_017009794.2:c.3471C>T
|
XP_016865283.1:p.Gly1157=
|
|
XR_427778.3:n.3882C>T
|
|
|
XR_427780.3:n.3771C>T
|
|
|
NM_000356.4:c.3531C>T
|
NP_000347.2:p.Gly1177=
|
|
NM_001135244.2:c.3651C>T
|
NP_001128716.1:p.Gly1217=
|
|
NM_001135245.2:c.3534C>T
|
NP_001128717.1:p.Gly1178=
|
|
NM_001195141.2:c.3648C>T
|
NP_001182070.1:p.Gly1216=
|
|
NM_001371623.1:c.3765C>T
MANE Select
|
NP_001358552.1:p.Gly1255=
|
|
NM_001135243.2:c.3762C>T
|
NP_001128715.1:p.Gly1254=
|
|