ENST00000361682.11:c.576C>T
MANE Select
|
ENSP00000354511.6:p.His192=
|
|
ENST00000428707.2:c.576C>T
|
ENSP00000387695.2:p.His192=
|
|
ENST00000676678.1:c.576C>T
|
ENSP00000503719.1:p.His192=
|
|
ENST00000677397.1:c.426C>T
|
ENSP00000503422.1:p.His142=
|
|
ENST00000677470.1:n.426C>T
|
|
|
ENST00000677564.1:n.359C>T
|
|
|
ENST00000677675.1:n.376C>T
|
|
|
ENST00000678240.1:n.424C>T
|
|
|
ENST00000678255.1:c.576C>T
|
ENSP00000504402.1:p.His192=
|
|
ENST00000678769.1:c.576C>T
|
ENSP00000503289.1:p.His192=
|
|
ENST00000678868.1:c.576C>T
|
ENSP00000503583.1:p.His192=
|
|
ENST00000678945.1:n.444C>T
|
|
|
ENST00000207636.9:c.*34C>T
|
ENSP00000207636.5:n.*34C>T
|
|
ENST00000361682.10:c.576C>T
|
ENSP00000354511.6:p.His192=
|
|
ENST00000403184.5:c.576C>T
|
ENSP00000383966.1:p.His192=
|
|
ENST00000403710.5:c.576C>T
|
ENSP00000385917.1:p.His192=
|
|
ENST00000406520.7:c.576C>T
|
ENSP00000385150.3:p.His192=
|
|
ENST00000407537.5:c.576C>T
|
ENSP00000384654.2:p.His192=
|
|
ENST00000412786.5:c.576C>T
|
ENSP00000403958.1:p.His192=
|
|
ENST00000428707.1:c.154C>T
|
|
|
ENST00000449653.5:c.426C>T
|
ENSP00000416778.1:p.His142=
|
|
ENST00000493893.1:n.314C>T
|
|
|
NM_000754.3:c.576C>T
|
NP_000745.1:p.His192=
|
|
NM_001135161.1:c.576C>T
|
NP_001128633.1:p.His192=
|
|
NM_001135162.1:c.576C>T
|
NP_001128634.1:p.His192=
|
|
NM_007310.2:c.426C>T
|
NP_009294.1:p.His142=
|
|
XM_011529885.1:c.690C>T
|
XP_011528187.1:p.His230=
|
|
XM_011529886.1:c.690C>T
|
XP_011528188.1:p.His230=
|
|
XM_011529887.1:c.576C>T
|
XP_011528189.1:p.His192=
|
|
XM_011529888.1:c.576C>T
|
XP_011528190.1:p.His192=
|
|
XM_011529889.1:c.576C>T
|
XP_011528191.1:p.His192=
|
|
XM_011529890.1:c.576C>T
|
XP_011528192.1:p.His192=
|
|
XM_011529891.1:c.576C>T
|
XP_011528193.1:p.His192=
|
|
NM_001362828.1:c.576C>T
|
NP_001349757.1:p.His192=
|
|
XM_011529886.2:c.987C>T
|
XP_011528188.2:p.His329=
|
|
XM_017028595.1:c.576C>T
|
XP_016884084.1:p.His192=
|
|
NM_000754.4:c.576C>T
MANE Select
|
NP_000745.1:p.His192=
|
|
NM_001135161.2:c.576C>T
|
NP_001128633.1:p.His192=
|
|
NM_001135162.2:c.576C>T
|
NP_001128634.1:p.His192=
|
|
NM_001362828.2:c.576C>T
|
NP_001349757.1:p.His192=
|
|
NM_007310.3:c.426C>T
|
NP_009294.1:p.His142=
|
|