ENST00000389048.8:c.3604G=
MANE Select
|
ENSP00000373700.3:p.Gly1202=
|
|
ENST00000431873.6:c.831G=
|
|
|
ENST00000638605.1:n.481G=
|
|
|
ENST00000642122.1:c.400G=
|
ENSP00000493203.1:p.Gly134=
|
|
ENST00000389048.7:c.3604G=
|
ENSP00000373700.3:p.Gly1202=
|
|
ENST00000431873.5:c.484G=
|
ENSP00000414027.2:p.Gly162=
|
|
ENST00000618119.4:c.2473G=
|
ENSP00000482733.1:p.Gly825=
|
|
NM_004304.4:c.3604G=
|
NP_004295.2:p.Gly1202=
|
|
NM_001353765.1:c.400G=
|
NP_001340694.1:p.Gly134=
|
|
XM_024452778.1:c.757G=
|
XP_024308546.1:p.Gly253=
|
|
XM_024452779.1:c.400G=
|
XP_024308547.1:p.Gly134=
|
|
NM_004304.5:c.3604G=
MANE Select
|
NP_004295.2:p.Gly1202=
|
|
NM_001353765.2:c.400G=
|
NP_001340694.1:p.Gly134=
|
|