|
NM_004119.3:c.2492G>C
MANE Select
|
NP_004110.2:p.Gly831Ala
|
|
ENST00000241453.12:c.2492G>C
MANE Select
|
ENSP00000241453.7:p.Gly831Ala
|
|
NM_004119.2:c.2492G>C , LRG_457t1:c.2492G>C
|
NP_004110.2:p.Gly831Ala
|
|
NR_130706.1:n.2706G>C
|
|
|
NR_130706.2:n.2690G>C
|
|
|
ENST00000241453.11:c.2492G>C
|
ENSP00000241453.7:p.Gly831Ala
|
|
ENST00000380987.2:c.*404G>C
|
ENSP00000370374.2:n.*404G>C
|
|
XM_011535015.1:c.2435G>C
|
XP_011533317.1:p.Gly812Ala
|
|
XM_011535015.2:c.2435G>C
|
XP_011533317.1:p.Gly812Ala
|
|
XM_011535016.1:c.1967G>C
|
XP_011533318.1:p.Gly656Ala
|
|
XM_011535017.1:c.1967G>C
|
XP_011533319.1:p.Gly656Ala
|
|
XM_011535017.2:c.1967G>C
|
XP_011533319.1:p.Gly656Ala
|
|
XM_011535018.1:c.1967G>C
|
XP_011533320.1:p.Gly656Ala
|
|
XM_011535018.2:c.1967G>C
|
XP_011533320.1:p.Gly656Ala
|
|
XM_017020486.1:c.2276G>C
|
XP_016875975.1:p.Gly759Ala
|
|
XM_017020487.1:c.1967G>C
|
XP_016875976.1:p.Gly656Ala
|
|
XM_017020488.1:c.1613G>C
|
XP_016875977.1:p.Gly538Ala
|
|
XM_017020489.1:c.1595G>C
|
XP_016875978.1:p.Gly532Ala
|
