|
NM_032119.4:c.16226G>A
MANE Select
|
NP_115495.3:p.Arg5409Gln
|
|
ENST00000405460.9:c.16226G>A
MANE Select
|
ENSP00000384582.2:p.Arg5409Gln
|
|
NM_032119.3:c.16226G>A
|
NP_115495.3:p.Arg5409Gln
|
|
NR_003149.1:n.16239G>A
|
|
|
NR_003149.2:n.16242G>A
|
|
|
ENST00000405460.6:c.16226G>A
|
ENSP00000384582.2:p.Arg5409Gln
|
|
ENST00000425867.2:c.3209G>A
|
ENSP00000392618.2:p.Arg1070Gln
|
|
ENST00000425867.3:c.5180G>A
|
ENSP00000392618.3:p.Arg1727Gln
|
|
ENST00000638510.1:n.3493G>A
|
|
|
ENST00000639431.1:c.265+147245G>A
|
ENSP00000491057.1:n.265+147245G>A
|
|
ENST00000640061.1:n.128+1272G>A
|
|
|
ENST00000640407.1:c.2636G>A
|
ENSP00000491425.1:p.Arg879Gln
|
|
XM_011543675.1:c.16223G>A
|
XP_011541977.1:p.Arg5408Gln
|
|
XM_011543676.1:c.16145G>A
|
XP_011541978.1:p.Arg5382Gln
|
|
XM_011543677.1:c.13529G>A
|
XP_011541979.1:p.Arg4510Gln
|
|
XM_017009963.2:c.16247G>A
|
XP_016865452.1:p.Arg5416Gln
|
|
XM_017009964.2:c.16244G>A
|
XP_016865453.1:p.Arg5415Gln
|
|
XM_017009965.1:c.16244G>A
|
XP_016865454.1:p.Arg5415Gln
|
|
XM_017009966.2:c.16166G>A
|
XP_016865455.1:p.Arg5389Gln
|
|
XM_017009967.1:c.16151G>A
|
XP_016865456.1:p.Arg5384Gln
|
|
XM_017009968.2:c.16067G>A
|
XP_016865457.1:p.Arg5356Gln
|
|
XM_017009969.2:c.16247G>A
|
XP_016865458.1:p.Arg5416Gln
|
|
XM_017009972.1:c.9365G>A
|
XP_016865461.1:p.Arg3122Gln
|
|
XM_017009973.1:c.9344G>A
|
XP_016865462.1:p.Arg3115Gln
|