|
ENST00000300417.11:c.1927A=
MANE Select
|
ENSP00000300417.6:p.Met643=
|
|
|
ENST00000472068.2:c.*1651A=
|
ENSP00000501555.1:n.*1651A=
|
|
|
ENST00000483302.6:n.2592A=
|
|
|
|
ENST00000498513.6:c.*818A=
|
ENSP00000501637.1:n.*818A=
|
|
|
ENST00000674511.1:n.1526A=
|
|
|
|
ENST00000674516.1:c.*543A=
|
ENSP00000502441.1:n.*543A=
|
|
|
ENST00000674621.1:n.1861-2349A=
|
|
|
|
ENST00000674771.1:c.*570A=
|
ENSP00000502627.1:n.*570A=
|
|
|
ENST00000674784.1:c.*987A=
|
ENSP00000501837.1:n.*987A=
|
|
|
ENST00000674970.1:c.*1701A=
|
ENSP00000502493.1:n.*1701A=
|
|
|
ENST00000675012.1:n.1871A=
|
|
|
|
ENST00000675141.1:c.1828A=
|
ENSP00000502420.1:p.Met610=
|
|
|
ENST00000675198.1:n.1807A=
|
|
|
|
ENST00000675213.1:c.1882A=
|
ENSP00000502218.1:p.Met628=
|
|
|
ENST00000675224.1:c.1955A=
|
ENSP00000501869.1:p.Asn652=
|
|
|
ENST00000675253.1:c.*599A=
|
ENSP00000502557.1:n.*599A=
|
|
|
ENST00000675445.1:c.*1599A=
|
ENSP00000502253.1:n.*1599A=
|
|
|
ENST00000675448.1:c.1927A=
|
ENSP00000502167.1:p.Met643=
|
|
|
ENST00000675521.1:n.1837A=
|
|
|
|
ENST00000675572.1:c.1828A=
|
ENSP00000501598.1:p.Met610=
|
|
|
ENST00000675641.1:c.*669A=
|
ENSP00000501845.1:n.*669A=
|
|
|
ENST00000675657.1:c.*540A=
|
ENSP00000502002.1:n.*540A=
|
|
|
ENST00000675662.1:n.1722A=
|
|
|
|
ENST00000675789.1:c.1747A=
|
ENSP00000501954.1:p.Met583=
|
|
|
ENST00000675883.1:c.1846A=
|
ENSP00000501592.1:p.Met616=
|
|
|
ENST00000675945.1:c.*568A=
|
ENSP00000501835.1:n.*568A=
|
|
|
ENST00000676014.1:c.1870A=
|
ENSP00000502058.1:p.Met624=
|
|
|
ENST00000676035.1:n.1589A=
|
|
|
|
ENST00000676106.1:n.1964A=
|
|
|
|
ENST00000676137.1:n.1957A=
|
|
|
|
ENST00000676170.1:c.2008A=
|
ENSP00000502177.1:p.Met670=
|
|
|
ENST00000676318.1:c.*2757A=
|
ENSP00000502300.1:n.*2757A=
|
|
|
ENST00000676336.1:c.*540A=
|
ENSP00000502686.1:n.*540A=
|
|
|
ENST00000676349.1:c.*1615A=
|
ENSP00000502155.1:n.*1615A=
|
|
|
ENST00000676399.1:n.1830A=
|
|
|
|
ENST00000676409.1:n.1987A=
|
|
|
|
ENST00000300417.10:c.1927A=
|
ENSP00000300417.6:p.Met643=
|
|
|
ENST00000323301.8:c.1927A=
|
ENSP00000322937.4:p.Met643=
|
|
|
ENST00000373322.1:c.1927A=
|
ENSP00000362419.1:p.Met643=
|
|
|
ENST00000373324.8:c.1846A=
|
ENSP00000362421.4:p.Met616=
|
|
|
ENST00000472068.1:n.820A=
|
|
|
|
ENST00000483302.5:n.1149A=
|
|
|
|
NM_001005373.3:c.1927A=
|
NP_001005373.1:p.Met643=
|
|
|
NM_001005374.3:c.1927A=
|
NP_001005374.1:p.Met643=
|
|
|
NM_001190723.2:c.1846A=
|
NP_001177652.1:p.Met616=
|
|
|
NM_138361.5:c.1927A= , LRG_373t1:c.1927A=
|
NP_612370.3:p.Met643=
|
|
|
XM_006717316.2:c.1828A=
|
XP_006717379.1:p.Met610=
|
|
|
XM_006717316.4:c.1828A=
|
XP_006717379.1:p.Met610=
|
|
|
XM_017015283.1:c.1927A=
|
XP_016870772.1:p.Met643=
|
|
|
XM_017015284.2:c.1138A=
|
XP_016870773.1:p.Met380=
|
|
|
XR_001746415.2:n.2462A=
|
|
|
|
XR_929874.3:n.2286A=
|
|
|
|
NM_001190723.3:c.1846A=
|
NP_001177652.1:p.Met616=
|
|
|
NM_001005373.4:c.1927A=
MANE Select
|
NP_001005373.1:p.Met643=
|
|
|
NM_001005374.4:c.1927A=
|
NP_001005374.1:p.Met643=
|
|
|
NM_001384142.1:c.1927A=
|
NP_001371071.1:p.Met643=
|
|
|
NM_001384143.1:c.1828A=
|
NP_001371072.1:p.Met610=
|
|
|
NM_001384144.1:c.1138A=
|
NP_001371073.1:p.Met380=
|
|
|
NR_168891.1:n.2456A=
|
|
|
|
NR_168892.1:n.2280A=
|
|
|
