ENST00000350026.11:c.3912C>T
|
ENSP00000055163.8:p.Ile1304=
|
|
ENST00000414678.8:c.3981C>T
|
ENSP00000412835.3:p.Ile1327=
|
|
ENST00000637015.2:c.4200C>T
|
ENSP00000489729.2:p.Ile1400=
|
|
ENST00000346085.10:c.3951C>T
|
ENSP00000344546.5:p.Ile1317=
|
|
ENST00000350026.10:c.3663C>T
|
ENSP00000055163.7:p.Ile1221=
|
|
ENST00000414678.7:c.2229C>T
|
ENSP00000412835.2:p.Ile743=
|
|
ENST00000635849.1:c.1392C>T
|
ENSP00000490948.1:p.Ile464=
|
|
ENST00000635957.1:c.1023C>T
|
ENSP00000490385.1:p.Ile341=
|
|
ENST00000636930.2:c.4071C>T
MANE Select
|
ENSP00000490491.2:p.Ile1357=
|
|
ENST00000636940.1:n.2068C>T
|
|
|
ENST00000637015.1:c.1439C>T
|
|
|
ENST00000637568.1:c.1353C>T
|
|
|
ENST00000637741.1:n.737C>T
|
|
|
ENST00000637810.1:c.1413C>T
|
ENSP00000489636.1:p.Ile471=
|
|
ENST00000637904.1:c.1572C>T
|
ENSP00000490550.1:p.Ile524=
|
|
ENST00000647938.1:c.3702C>T
|
ENSP00000498155.1:p.Ile1234=
|
|
ENST00000346085.9:c.3702C>T
|
ENSP00000344546.4:p.Ile1234=
|
|
ENST00000350026.9:c.3663C>T
|
ENSP00000055163.7:p.Ile1221=
|
|
ENST00000414678.6:c.2229C>T
|
ENSP00000412835.2:p.Ile743=
|
|
NM_017519.2:c.3663C>T
|
NP_059989.2:p.Ile1221=
|
|
NM_020732.3:c.3702C>T
|
NP_065783.3:p.Ile1234=
|
|
XM_005267069.3:c.3822C>T
|
XP_005267126.2:p.Ile1274=
|
|
XM_011535984.1:c.2901C>T
|
XP_011534286.1:p.Ile967=
|
|
XM_011535985.1:c.2721C>T
|
XP_011534287.1:p.Ile907=
|
|
XM_011535986.1:c.2481C>T
|
XP_011534288.1:p.Ile827=
|
|
XM_011535987.1:c.2100C>T
|
XP_011534289.1:p.Ile700=
|
|
XM_011535988.1:c.963C>T
|
XP_011534290.1:p.Ile321=
|
|
NM_001346813.1:c.3822C>T
|
NP_001333742.1:p.Ile1274=
|
|
NM_001363725.1:c.1572C>T
|
NP_001350654.1:p.Ile524=
|
|
XM_011535984.2:c.4032C>T
|
XP_011534286.2:p.Ile1344=
|
|
XM_011535988.3:c.963C>T
|
XP_011534290.1:p.Ile321=
|
|
XM_017011103.2:c.3933C>T
|
XP_016866592.1:p.Ile1311=
|
|
XM_017011104.1:c.3903C>T
|
XP_016866593.1:p.Ile1301=
|
|
XM_017011105.2:c.3873C>T
|
XP_016866594.1:p.Ile1291=
|
|
XM_017011106.2:c.3744C>T
|
XP_016866595.1:p.Ile1248=
|
|
XM_017011107.2:c.3723C>T
|
XP_016866596.1:p.Ile1241=
|
|
XR_002956289.1:n.4115C>T
|
|
|
NM_001363725.2:c.1572C>T
|
NP_001350654.1:p.Ile524=
|
|
NM_001371656.1:c.3951C>T
|
NP_001358585.1:p.Ile1317=
|
|
NM_001374820.1:c.3951C>T
|
NP_001361749.1:p.Ile1317=
|
|
NM_001374828.1:c.4071C>T
MANE Select
|
NP_001361757.1:p.Ile1357=
|
|
NM_017519.3:c.3912C>T
|
NP_059989.3:p.Ile1304=
|
|