ENST00000241453.12:c.2427C>G
MANE Select
|
ENSP00000241453.7:p.His809Gln
|
|
ENST00000241453.11:c.2427C>G
|
ENSP00000241453.7:p.His809Gln
|
|
ENST00000380987.2:c.*339C>G
|
ENSP00000370374.2:n.*339C>G
|
|
NM_004119.2:c.2427C>G , LRG_457t1:c.2427C>G
|
NP_004110.2:p.His809Gln
|
|
NR_130706.1:n.2641C>G
|
|
|
XM_011535015.1:c.2370C>G
|
XP_011533317.1:p.His790Gln
|
|
XM_011535016.1:c.1902C>G
|
XP_011533318.1:p.His634Gln
|
|
XM_011535017.1:c.1902C>G
|
XP_011533319.1:p.His634Gln
|
|
XM_011535018.1:c.1902C>G
|
XP_011533320.1:p.His634Gln
|
|
XM_011535015.2:c.2370C>G
|
XP_011533317.1:p.His790Gln
|
|
XM_011535017.2:c.1902C>G
|
XP_011533319.1:p.His634Gln
|
|
XM_011535018.2:c.1902C>G
|
XP_011533320.1:p.His634Gln
|
|
XM_017020486.1:c.2211C>G
|
XP_016875975.1:p.His737Gln
|
|
XM_017020487.1:c.1902C>G
|
XP_016875976.1:p.His634Gln
|
|
XM_017020488.1:c.1548C>G
|
XP_016875977.1:p.His516Gln
|
|
XM_017020489.1:c.1530C>G
|
XP_016875978.1:p.His510Gln
|
|
NM_004119.3:c.2427C>G
MANE Select
|
NP_004110.2:p.His809Gln
|
|
NR_130706.2:n.2625C>G
|
|
|