|
ENST00000507116.6:c.1570A>G
|
ENSP00000424852.1:p.Met524Val
|
|
|
ENST00000340635.11:c.1762A>G
MANE Select
|
ENSP00000345502.6:p.Met588Val
|
|
|
ENST00000636120.1:c.1432A>G
|
ENSP00000490821.1:p.Met478Val
|
|
|
ENST00000309641.10:c.1614A>G
|
ENSP00000308485.6:n.1614A>G
|
|
|
ENST00000317118.12:c.889A>G
|
ENSP00000321739.8:p.Met297Val
|
|
|
ENST00000340635.10:c.1762A>G
|
ENSP00000345502.6:p.Met588Val
|
|
|
ENST00000358923.10:c.856A>G
|
ENSP00000351800.6:p.Met286Val
|
|
|
ENST00000360047.9:c.1354A>G
|
ENSP00000353152.5:p.Met452Val
|
|
|
ENST00000405755.6:c.1396A>G
|
ENSP00000384806.2:p.Met466Val
|
|
|
ENST00000502484.6:c.1579A>G
|
ENSP00000423094.2:p.Met527Val
|
|
|
ENST00000503258.5:c.1372A>G
|
ENSP00000425605.1:p.Met458Val
|
|
|
ENST00000505453.1:c.856A>G
|
ENSP00000421013.1:p.Met286Val
|
|
|
ENST00000507116.5:c.1570A>G
|
ENSP00000424852.1:p.Met524Val
|
|
|
ENST00000515011.5:n.1498A>G
|
|
|
|
ENST00000546160.5:c.1369A>G
|
ENSP00000442734.2:p.Met457Val
|
|
|
NM_001104631.1:c.1762A>G
|
NP_001098101.1:p.Met588Val
|
|
|
NM_001165899.1:c.1579A>G
|
NP_001159371.1:p.Met527Val
|
|
|
NM_001197218.1:c.1570A>G
|
NP_001184147.1:p.Met524Val
|
|
|
NM_001197219.1:c.1396A>G
|
NP_001184148.1:p.Met466Val
|
|
|
NM_001197220.1:c.1372A>G
|
NP_001184149.1:p.Met458Val
|
|
|
NM_001197221.1:c.856A>G
|
NP_001184150.1:p.Met286Val
|
|
|
NM_001197222.1:c.1090A>G
|
NP_001184151.1:p.Met364Val
|
|
|
NM_001197223.1:c.889A>G
|
NP_001184152.1:p.Met297Val
|
|
|
NM_006203.4:c.1354A>G
|
NP_006194.2:p.Met452Val
|
|
|
XM_005248537.2:c.1432A>G
|
XP_005248594.1:p.Met478Val
|
|
|
XM_005248538.3:c.1354A>G
|
XP_005248595.1:p.Met452Val
|
|
|
XM_011543469.1:c.1726A>G
|
XP_011541771.1:p.Met576Val
|
|
|
XM_011543470.1:c.1726A>G
|
XP_011541772.1:p.Met576Val
|
|
|
XM_011543471.1:c.1579A>G
|
XP_011541773.1:p.Met527Val
|
|
|
XM_011543472.1:c.1579A>G
|
XP_011541774.1:p.Met527Val
|
|
|
XM_011543473.1:c.1579A>G
|
XP_011541775.1:p.Met527Val
|
|
|
XM_011543474.1:c.1549A>G
|
XP_011541776.1:p.Met517Val
|
|
|
XM_011543475.1:c.1396A>G
|
XP_011541777.1:p.Met466Val
|
|
|
XM_011543476.1:c.1342A>G
|
XP_011541778.1:p.Met448Val
|
|
|
XM_011543477.1:c.1321A>G
|
XP_011541779.1:p.Met441Val
|
|
|
XM_011543478.1:c.1258A>G
|
XP_011541780.1:p.Met420Val
|
|
|
XM_011543479.1:c.1258A>G
|
XP_011541781.1:p.Met420Val
|
|
|
NM_001349241.1:c.1549A>G
|
NP_001336170.1:p.Met517Val
|
|
|
NM_001349242.1:c.1432A>G
|
NP_001336171.1:p.Met478Val
|
|
|
NM_001349243.1:c.994A>G
|
NP_001336172.1:p.Met332Val
|
|
|
NM_001364599.1:c.1579A>G
|
NP_001351528.1:p.Met527Val
|
|
|
NM_001364603.1:c.856A>G
|
NP_001351532.1:p.Met286Val
|
|
|
NM_001364604.1:c.994A>G
|
NP_001351533.1:p.Met332Val
|
|
|
XM_011543470.2:c.1726A>G
|
XP_011541772.1:p.Met576Val
|
|
|
XM_011543471.2:c.1579A>G
|
XP_011541773.1:p.Met527Val
|
|
|
XM_017009565.1:c.1726A>G
|
XP_016865054.1:p.Met576Val
|
|
|
XM_017009566.1:c.1579A>G
|
XP_016865055.1:p.Met527Val
|
|
|
XM_017009567.1:c.1564A>G
|
XP_016865056.1:p.Met522Val
|
|
|
XM_024446110.1:c.1726A>G
|
XP_024301878.1:p.Met576Val
|
|
|
XM_024446112.1:c.1579A>G
|
XP_024301880.1:p.Met527Val
|
|
|
NM_001104631.2:c.1762A>G
MANE Select
|
NP_001098101.1:p.Met588Val
|
|
|
NM_001165899.2:c.1579A>G
|
NP_001159371.1:p.Met527Val
|
|
|
NM_001197218.2:c.1570A>G
|
NP_001184147.1:p.Met524Val
|
|
|
NM_001197219.2:c.1396A>G
|
NP_001184148.1:p.Met466Val
|
|
|
NM_001197220.2:c.1372A>G
|
NP_001184149.1:p.Met458Val
|
|
|
NM_001197221.2:c.856A>G
|
NP_001184150.1:p.Met286Val
|
|
|
NM_001197222.2:c.1090A>G
|
NP_001184151.1:p.Met364Val
|
|
|
NM_001197223.2:c.889A>G
|
NP_001184152.1:p.Met297Val
|
|
|
NM_001349241.2:c.1549A>G
|
NP_001336170.1:p.Met517Val
|
|
|
NM_001349243.2:c.994A>G
|
NP_001336172.1:p.Met332Val
|
|
|
NM_001349242.2:c.1432A>G
|
NP_001336171.1:p.Met478Val
|
|
|
NM_006203.5:c.1354A>G
|
NP_006194.2:p.Met452Val
|
|
