ENST00000617695.5:c.7711A>C
|
ENSP00000481744.2:p.Arg2571=
|
|
ENST00000618192.5:c.7987A>C
|
ENSP00000480802.2:p.Arg2663=
|
|
ENST00000421865.3:c.7723A>C
MANE Select
|
ENSP00000400365.2:p.Arg2575=
|
|
ENST00000421865.2:c.7723A>C
|
ENSP00000400365.2:p.Arg2575=
|
|
ENST00000617695.4:c.7711A>C
|
ENSP00000481744.1:p.Arg2571=
|
|
ENST00000618192.4:c.7720A>C
|
ENSP00000480802.1:p.Arg2574=
|
|
NM_000426.3:c.7723A>C , LRG_409t1:c.7723A>C
|
NP_000417.2:p.Arg2575=
|
|
NM_001079823.1:c.7711A>C
|
NP_001073291.1:p.Arg2571=
|
|
XM_005266981.2:c.7987A>C
|
XP_005267038.1:p.Arg2663=
|
|
XM_005266982.2:c.7975A>C
|
XP_005267039.1:p.Arg2659=
|
|
XM_011535820.1:c.7981A>C
|
XP_011534122.1:p.Arg2661=
|
|
XM_005266981.3:c.7987A>C
|
XP_005267038.1:p.Arg2663=
|
|
XM_005266982.3:c.7975A>C
|
XP_005267039.1:p.Arg2659=
|
|
XM_011535820.2:c.7981A>C
|
XP_011534122.1:p.Arg2661=
|
|
XM_017010851.2:c.7993A>C
|
XP_016866340.1:p.Arg2665=
|
|
XM_017010852.1:c.6118A>C
|
XP_016866341.1:p.Arg2040=
|
|
NM_000426.4:c.7723A>C
MANE Select
|
NP_000417.3:p.Arg2575=
|
|
NM_001079823.2:c.7711A>C
|
NP_001073291.2:p.Arg2571=
|
|