|
NM_032119.4:c.12919G>A
MANE Select
|
NP_115495.3:p.Gly4307Arg
|
|
ENST00000405460.9:c.12919G>A
MANE Select
|
ENSP00000384582.2:p.Gly4307Arg
|
|
NM_032119.3:c.12919G>A
|
NP_115495.3:p.Gly4307Arg
|
|
NR_003149.1:n.12932G>A
|
|
|
NR_003149.2:n.12935G>A
|
|
|
ENST00000405460.6:c.12919G>A
|
ENSP00000384582.2:p.Gly4307Arg
|
|
ENST00000425867.3:c.1873G>A
|
ENSP00000392618.3:p.Gly625Arg
|
|
ENST00000639431.1:c.265+102725G>A
|
ENSP00000491057.1:n.265+102725G>A
|
|
ENST00000640464.1:n.3338G>A
|
|
|
XM_011543675.1:c.12916G>A
|
XP_011541977.1:p.Gly4306Arg
|
|
XM_011543676.1:c.12838G>A
|
XP_011541978.1:p.Gly4280Arg
|
|
XM_011543677.1:c.10222G>A
|
XP_011541979.1:p.Gly3408Arg
|
|
XM_011543678.1:c.12919G>A
|
XP_011541980.1:p.Gly4307Arg
|
|
XM_017009963.2:c.12940G>A
|
XP_016865452.1:p.Gly4314Arg
|
|
XM_017009964.2:c.12937G>A
|
XP_016865453.1:p.Gly4313Arg
|
|
XM_017009965.1:c.12937G>A
|
XP_016865454.1:p.Gly4313Arg
|
|
XM_017009966.2:c.12859G>A
|
XP_016865455.1:p.Gly4287Arg
|
|
XM_017009967.1:c.12844G>A
|
XP_016865456.1:p.Gly4282Arg
|
|
XM_017009968.2:c.12940G>A
|
XP_016865457.1:p.Gly4314Arg
|
|
XM_017009969.2:c.12940G>A
|
XP_016865458.1:p.Gly4314Arg
|
|
XM_017009970.2:c.12940G>A
|
XP_016865459.1:p.Gly4314Arg
|
|
XM_017009971.2:c.12940G>A
|
XP_016865460.1:p.Gly4314Arg
|
|
XM_017009972.1:c.6058G>A
|
XP_016865461.1:p.Gly2020Arg
|
|
XM_017009973.1:c.6037G>A
|
XP_016865462.1:p.Gly2013Arg
|