ENST00000346322.10:c.4400T>C
|
ENSP00000320622.6:p.Met1467Thr
|
|
ENST00000508240.2:c.1007T>C
|
ENSP00000422984.2:p.Met336Thr
|
|
ENST00000513111.2:n.737T>C
|
|
|
ENST00000684879.1:n.2239T>C
|
|
|
ENST00000685021.1:c.1841T>C
|
ENSP00000508447.1:p.Met614Thr
|
|
ENST00000685259.1:c.2126T>C
|
|
|
ENST00000685907.1:n.2388T>C
|
|
|
ENST00000685953.1:c.1007T>C
|
ENSP00000510593.1:p.Met336Thr
|
|
ENST00000686039.1:c.1991T>C
|
|
|
ENST00000686245.1:c.1724T>C
|
ENSP00000509313.1:p.Met575Thr
|
|
ENST00000686406.1:c.4607T>C
|
ENSP00000509044.1:p.Met1536Thr
|
|
ENST00000686458.1:n.1109T>C
|
|
|
ENST00000686761.1:c.4607T>C
|
ENSP00000508758.1:p.Met1536Thr
|
|
ENST00000686822.1:n.4501T>C
|
|
|
ENST00000687434.1:c.*823T>C
|
ENSP00000509751.1:n.*823T>C
|
|
ENST00000687709.1:n.2662T>C
|
|
|
ENST00000687848.1:c.4637T>C
|
ENSP00000508761.1:p.Met1546Thr
|
|
ENST00000688024.1:c.1841T>C
|
ENSP00000509803.1:p.Met614Thr
|
|
ENST00000688223.1:c.1649+1735T>C
|
ENSP00000508935.1:n.1649+1735T>C
|
|
ENST00000689868.1:n.2335T>C
|
|
|
ENST00000689918.1:n.682T>C
|
|
|
ENST00000690086.1:n.708T>C
|
|
|
ENST00000690167.1:n.2278T>C
|
|
|
ENST00000690457.1:c.3845T>C
|
ENSP00000508777.1:p.Met1282Thr
|
|
ENST00000690534.1:n.1128T>C
|
|
|
ENST00000691933.1:c.2231T>C
|
|
|
ENST00000692352.1:c.2145T>C
|
|
|
ENST00000693689.1:c.4400T>C
|
ENSP00000510503.1:p.Met1467Thr
|
|
ENST00000360304.8:c.4607T>C
MANE Select
|
ENSP00000353452.3:p.Met1536Thr
|
|
ENST00000346322.9:c.4400T>C
|
ENSP00000320622.5:p.Met1467Thr
|
|
ENST00000354792.9:c.4400T>C
|
ENSP00000346846.6:p.Met1467Thr
|
|
ENST00000359169.5:c.4607T>C
|
ENSP00000352088.1:p.Met1536Thr
|
|
ENST00000360304.7:c.4607T>C
|
ENSP00000353452.3:p.Met1536Thr
|
|
ENST00000360772.7:c.4607T>C
|
ENSP00000354004.3:p.Met1536Thr
|
|
ENST00000464489.5:c.*4186T>C
|
ENSP00000417798.1:n.*4186T>C
|
|
ENST00000475616.5:c.4607T>C
|
ENSP00000418335.1:p.Met1536Thr
|
|
ENST00000513111.1:n.319T>C
|
|
|
ENST00000514895.5:n.94+1735T>C
|
|
|
NM_053025.3:c.4607T>C
|
NP_444253.3:p.Met1536Thr
|
|
NM_053026.3:c.4400T>C
|
NP_444254.3:p.Met1467Thr
|
|
NM_053027.3:c.4607T>C
|
NP_444255.3:p.Met1536Thr
|
|
NM_053028.3:c.4400T>C
|
NP_444256.3:p.Met1467Thr
|
|
XM_011512860.1:c.4607T>C
|
XP_011511162.1:p.Met1536Thr
|
|
XM_011512861.1:c.4415+1735T>C
|
XP_011511163.1:n.4415+1735T>C
|
|
XM_011512862.1:c.4079T>C
|
XP_011511164.1:p.Met1360Thr
|
|
NM_001321309.1:c.4079T>C
|
NP_001308238.1:p.Met1360Thr
|
|
XM_011512860.3:c.4637T>C
|
XP_011511162.2:p.Met1546Thr
|
|
XM_011512861.3:c.4445+1735T>C
|
XP_011511163.2:n.4445+1735T>C
|
|
XM_017006469.2:c.1841T>C
|
XP_016861958.1:p.Met614Thr
|
|
XM_017006470.2:c.1007T>C
|
XP_016861959.1:p.Met336Thr
|
|
XM_017006471.2:c.1007T>C
|
XP_016861960.1:p.Met336Thr
|
|
XM_024453532.1:c.4637T>C
|
XP_024309300.1:p.Met1546Thr
|
|
XM_024453533.1:c.4607T>C
|
XP_024309301.1:p.Met1536Thr
|
|
XM_024453534.1:c.4430T>C
|
XP_024309302.1:p.Met1477Thr
|
|
XM_024453535.1:c.4400T>C
|
XP_024309303.1:p.Met1467Thr
|
|
XM_024453536.1:c.4607T>C
|
XP_024309304.1:p.Met1536Thr
|
|
XM_024453537.1:c.4607T>C
|
XP_024309305.1:p.Met1536Thr
|
|
NM_001321309.2:c.4079T>C
|
NP_001308238.1:p.Met1360Thr
|
|
NM_053025.4:c.4607T>C
MANE Select
|
NP_444253.3:p.Met1536Thr
|
|
NM_053026.4:c.4400T>C
|
NP_444254.3:p.Met1467Thr
|
|
NM_053027.4:c.4607T>C
|
NP_444255.3:p.Met1536Thr
|
|
NM_053028.4:c.4400T>C
|
NP_444256.3:p.Met1467Thr
|
|