|
ENST00000361874.8:c.3543G>T
|
ENSP00000354791.4:p.Met1181Ile
|
|
|
ENST00000628224.3:c.3558G>T
MANE Select
|
ENSP00000487279.2:p.Met1186Ile
|
|
|
ENST00000680606.1:c.3507G>T
|
ENSP00000505612.1:p.Met1169Ile
|
|
|
ENST00000361874.7:c.3558G>T
|
ENSP00000354791.3:p.Met1186Ile
|
|
|
ENST00000394003.7:c.3537G>T
|
ENSP00000377571.3:p.Met1179Ile
|
|
|
ENST00000409240.5:c.3432G>T
|
ENSP00000386406.1:p.Met1144Ile
|
|
|
ENST00000409438.5:c.3141G>T
|
ENSP00000387270.1:p.Met1047Ile
|
|
|
ENST00000409567.7:c.3483G>T
|
ENSP00000386843.3:p.Met1161Ile
|
|
|
ENST00000409868.5:c.3492G>T
|
ENSP00000387327.1:p.Met1164Ile
|
|
|
ENST00000434055.5:c.*842G>T
|
ENSP00000416711.1:n.*842G>T
|
|
|
ENST00000451608.2:c.297G>T
|
ENSP00000416453.2:p.Met99Ile
|
|
|
ENST00000466110.5:n.4795G>T
|
|
|
|
ENST00000491465.5:n.1821G>T
|
|
|
|
ENST00000492717.1:n.229G>T
|
|
|
|
ENST00000497666.1:n.97-1164G>T
|
|
|
|
ENST00000628224.2:c.3492G>T
|
ENSP00000487279.1:p.Met1164Ile
|
|
|
ENST00000633691.1:c.3156G>T
|
ENSP00000487724.1:p.Met1052Ile
|
|
|
NM_001135040.2:c.3483G>T
|
NP_001128512.1:p.Met1161Ile
|
|
|
NM_001135041.2:c.3141G>T
|
NP_001128513.1:p.Met1047Ile
|
|
|
NM_001190836.1:c.3432G>T
|
NP_001177765.1:p.Met1144Ile
|
|
|
NM_001190837.1:c.3537G>T
|
NP_001177766.1:p.Met1179Ile
|
|
|
NM_004082.4:c.3558G>T
|
NP_004073.2:p.Met1186Ile
|
|
|
NM_023019.3:c.3156G>T
|
NP_075408.1:p.Met1052Ile
|
|
|
NR_033935.1:n.3827G>T
|
|
|
|
NM_001135040.3:c.3483G>T
|
NP_001128512.1:p.Met1161Ile
|
|
|
NM_001135041.3:c.3141G>T
|
NP_001128513.1:p.Met1047Ile
|
|
|
NM_001190836.2:c.3432G>T
|
NP_001177765.1:p.Met1144Ile
|
|
|
NM_001190837.2:c.3537G>T
|
NP_001177766.1:p.Met1179Ile
|
|
|
NM_001378991.1:c.3507G>T
|
NP_001365920.1:p.Met1169Ile
|
|
|
NM_001378992.1:c.3489G>T
|
NP_001365921.1:p.Met1163Ile
|
|
|
NM_004082.5:c.3558G>T
MANE Select
|
NP_004073.2:p.Met1186Ile
|
|
|
NM_023019.4:c.3156G>T
|
NP_075408.1:p.Met1052Ile
|
|
|
NR_033935.2:n.3606G>T
|
|
|
