ENST00000294304.12:c.3973G>C
MANE Select
|
ENSP00000294304.6:p.Asp1325His
|
|
ENST00000294304.11:c.3973G>C
|
ENSP00000294304.6:p.Asp1325His
|
|
ENST00000529993.5:c.*2579G>C
|
ENSP00000436652.1:n.*2579G>C
|
|
NM_001291902.1:c.2230G>C
|
NP_001278831.1:p.Asp744His
|
|
NM_002335.3:c.3973G>C
|
NP_002326.2:p.Asp1325His
|
|
XM_005273994.2:c.3973G>C
|
XP_005274051.1:p.Asp1325His
|
|
XM_011545029.1:c.4000G>C
|
XP_011543331.1:p.Asp1334His
|
|
XM_011545030.1:c.4000G>C
|
XP_011543332.1:p.Asp1334His
|
|
XM_011545031.1:c.4000G>C
|
XP_011543333.1:p.Asp1334His
|
|
XR_949925.1:n.4015G>C
|
|
|
XR_949926.1:n.4015G>C
|
|
|
XM_017017735.1:c.2230G>C
|
XP_016873224.1:p.Asp744His
|
|
XM_017017736.1:c.1513G>C
|
XP_016873225.1:p.Asp505His
|
|
XR_949925.2:n.4015G>C
|
|
|
XR_949926.2:n.4015G>C
|
|
|
NM_002335.4:c.3973G>C
MANE Select
|
NP_002326.2:p.Asp1325His
|
|
NM_001291902.2:c.2230G>C
|
NP_001278831.1:p.Asp744His
|
|