ENST00000282849.10:c.1823G>C
MANE Select
|
ENSP00000282849.5:p.Gly608Ala
|
|
ENST00000282849.9:c.1823G>C
|
ENSP00000282849.5:p.Gly608Ala
|
|
NM_199355.2:c.1823G>C
|
NP_955387.1:p.Gly608Ala
|
|
XM_006721158.2:c.-93G>C
|
XP_006721221.1:n.-93G>C
|
|
XM_011522923.1:c.1307G>C
|
XP_011521225.1:p.Gly436Ala
|
|
XM_011522924.1:c.1307G>C
|
XP_011521226.1:p.Gly436Ala
|
|
NM_001326358.1:c.1307G>C
|
NP_001313287.1:p.Gly436Ala
|
|
NM_199355.3:c.1823G>C
|
NP_955387.1:p.Gly608Ala
|
|
XM_011522924.2:c.1307G>C
|
XP_011521226.1:p.Gly436Ala
|
|
XM_017022988.2:c.587G>C
|
XP_016878477.1:p.Gly196Ala
|
|
XM_017022989.1:c.587G>C
|
XP_016878478.1:p.Gly196Ala
|
|
NM_199355.4:c.1823G>C
MANE Select
|
NP_955387.1:p.Gly608Ala
|
|
NM_001326358.2:c.1307G>C
|
NP_001313287.1:p.Gly436Ala
|
|