|
ENST00000361682.11:c.269T=
MANE Select
|
ENSP00000354511.6:p.Met90=
|
|
|
ENST00000428707.2:c.269T=
|
ENSP00000387695.2:p.Met90=
|
|
|
ENST00000676678.1:c.269T=
|
ENSP00000503719.1:p.Met90=
|
|
|
ENST00000677397.1:c.119T=
|
ENSP00000503422.1:p.Met40=
|
|
|
ENST00000678240.1:n.117T=
|
|
|
|
ENST00000678255.1:c.269T=
|
ENSP00000504402.1:p.Met90=
|
|
|
ENST00000678769.1:c.269T=
|
ENSP00000503289.1:p.Met90=
|
|
|
ENST00000678868.1:c.269T=
|
ENSP00000503583.1:p.Met90=
|
|
|
ENST00000207636.9:c.269T=
|
ENSP00000207636.5:p.Met90=
|
|
|
ENST00000361682.10:c.269T=
|
ENSP00000354511.6:p.Met90=
|
|
|
ENST00000403184.5:c.269T=
|
ENSP00000383966.1:p.Met90=
|
|
|
ENST00000403710.5:c.269T=
|
ENSP00000385917.1:p.Met90=
|
|
|
ENST00000406520.7:c.269T=
|
ENSP00000385150.3:p.Met90=
|
|
|
ENST00000407537.5:c.269T=
|
ENSP00000384654.2:p.Met90=
|
|
|
ENST00000412786.5:c.269T=
|
ENSP00000403958.1:p.Met90=
|
|
|
ENST00000449653.5:c.119T=
|
ENSP00000416778.1:p.Met40=
|
|
|
ENST00000467943.5:n.465T=
|
|
|
|
NM_000754.3:c.269T=
|
NP_000745.1:p.Met90=
|
|
|
NM_001135161.1:c.269T=
|
NP_001128633.1:p.Met90=
|
|
|
NM_001135162.1:c.269T=
|
NP_001128634.1:p.Met90=
|
|
|
NM_007310.2:c.119T=
|
NP_009294.1:p.Met40=
|
|
|
XM_011529885.1:c.383T=
|
XP_011528187.1:p.Met128=
|
|
|
XM_011529886.1:c.383T=
|
XP_011528188.1:p.Met128=
|
|
|
XM_011529887.1:c.269T=
|
XP_011528189.1:p.Met90=
|
|
|
XM_011529888.1:c.269T=
|
XP_011528190.1:p.Met90=
|
|
|
XM_011529889.1:c.269T=
|
XP_011528191.1:p.Met90=
|
|
|
XM_011529890.1:c.269T=
|
XP_011528192.1:p.Met90=
|
|
|
XM_011529891.1:c.269T=
|
XP_011528193.1:p.Met90=
|
|
|
NM_001362828.1:c.269T=
|
NP_001349757.1:p.Met90=
|
|
|
XM_011529886.2:c.680T=
|
XP_011528188.2:p.Met227=
|
|
|
XM_017028595.1:c.269T=
|
XP_016884084.1:p.Met90=
|
|
|
NM_000754.4:c.269T=
MANE Select
|
NP_000745.1:p.Met90=
|
|
|
NM_001135161.2:c.269T=
|
NP_001128633.1:p.Met90=
|
|
|
NM_001135162.2:c.269T=
|
NP_001128634.1:p.Met90=
|
|
|
NM_001362828.2:c.269T=
|
NP_001349757.1:p.Met90=
|
|
|
NM_007310.3:c.119T=
|
NP_009294.1:p.Met40=
|
|
