ENST00000706094.1:c.1312G>C
|
ENSP00000516212.1:p.Gly438Arg
|
|
ENST00000374542.10:c.1276G>C
MANE Select
|
ENSP00000363668.5:p.Gly426Arg
|
|
ENST00000266000.10:c.1276G>C
|
ENSP00000266000.6:p.Gly426Arg
|
|
ENST00000374542.9:c.1276G>C
|
ENSP00000363668.5:p.Gly426Arg
|
|
ENST00000414083.6:c.1051G>C
|
ENSP00000396876.2:p.Gly351Arg
|
|
ENST00000468536.5:n.306G>C
|
|
|
ENST00000477162.1:n.388G>C
|
|
|
ENST00000490173.1:n.261G>C
|
|
|
ENST00000620164.4:c.1276G>C
|
ENSP00000482399.1:p.Gly426Arg
|
|
NM_001141969.1:c.1276G>C
|
NP_001135441.1:p.Gly426Arg
|
|
NM_001141970.1:c.1312G>C
|
NP_001135442.1:p.Gly438Arg
|
|
NM_001254717.1:c.1051G>C
|
NP_001241646.1:p.Gly351Arg
|
|
NM_001350.4:c.1276G>C
|
NP_001341.1:p.Gly426Arg
|
|
XM_005248860.3:c.172G>C
|
XP_005248917.1:p.Gly58Arg
|
|
NM_001141969.2:c.1276G>C
MANE Select
|
NP_001135441.1:p.Gly426Arg
|
|
NM_001141970.2:c.1312G>C
|
NP_001135442.1:p.Gly438Arg
|
|
NM_001350.5:c.1276G>C
|
NP_001341.1:p.Gly426Arg
|
|
NM_001254717.2:c.1051G>C
|
NP_001241646.1:p.Gly351Arg
|
|