ENST00000350026.11:c.3910A>T
|
ENSP00000055163.8:p.Ile1304Phe
|
|
ENST00000414678.8:c.3979A>T
|
ENSP00000412835.3:p.Ile1327Phe
|
|
ENST00000637015.2:c.4198A>T
|
ENSP00000489729.2:p.Ile1400Phe
|
|
ENST00000346085.10:c.3949A>T
|
ENSP00000344546.5:p.Ile1317Phe
|
|
ENST00000350026.10:c.3661A>T
|
ENSP00000055163.7:p.Ile1221Phe
|
|
ENST00000414678.7:c.2227A>T
|
ENSP00000412835.2:p.Ile743Phe
|
|
ENST00000635849.1:c.1390A>T
|
ENSP00000490948.1:p.Ile464Phe
|
|
ENST00000635957.1:c.1021A>T
|
ENSP00000490385.1:p.Ile341Phe
|
|
ENST00000636930.2:c.4069A>T
MANE Select
|
ENSP00000490491.2:p.Ile1357Phe
|
|
ENST00000636940.1:n.2066A>T
|
|
|
ENST00000637015.1:c.1437A>T
|
|
|
ENST00000637568.1:c.1351A>T
|
|
|
ENST00000637741.1:n.735A>T
|
|
|
ENST00000637810.1:c.1411A>T
|
ENSP00000489636.1:p.Ile471Phe
|
|
ENST00000637904.1:c.1570A>T
|
ENSP00000490550.1:p.Ile524Phe
|
|
ENST00000647938.1:c.3700A>T
|
ENSP00000498155.1:p.Ile1234Phe
|
|
ENST00000346085.9:c.3700A>T
|
ENSP00000344546.4:p.Ile1234Phe
|
|
ENST00000350026.9:c.3661A>T
|
ENSP00000055163.7:p.Ile1221Phe
|
|
ENST00000414678.6:c.2227A>T
|
ENSP00000412835.2:p.Ile743Phe
|
|
NM_017519.2:c.3661A>T
|
NP_059989.2:p.Ile1221Phe
|
|
NM_020732.3:c.3700A>T
|
NP_065783.3:p.Ile1234Phe
|
|
XM_005267069.3:c.3820A>T
|
XP_005267126.2:p.Ile1274Phe
|
|
XM_011535984.1:c.2899A>T
|
XP_011534286.1:p.Ile967Phe
|
|
XM_011535985.1:c.2719A>T
|
XP_011534287.1:p.Ile907Phe
|
|
XM_011535986.1:c.2479A>T
|
XP_011534288.1:p.Ile827Phe
|
|
XM_011535987.1:c.2098A>T
|
XP_011534289.1:p.Ile700Phe
|
|
XM_011535988.1:c.961A>T
|
XP_011534290.1:p.Ile321Phe
|
|
NM_001346813.1:c.3820A>T
|
NP_001333742.1:p.Ile1274Phe
|
|
NM_001363725.1:c.1570A>T
|
NP_001350654.1:p.Ile524Phe
|
|
XM_011535984.2:c.4030A>T
|
XP_011534286.2:p.Ile1344Phe
|
|
XM_011535988.3:c.961A>T
|
XP_011534290.1:p.Ile321Phe
|
|
XM_017011103.2:c.3931A>T
|
XP_016866592.1:p.Ile1311Phe
|
|
XM_017011104.1:c.3901A>T
|
XP_016866593.1:p.Ile1301Phe
|
|
XM_017011105.2:c.3871A>T
|
XP_016866594.1:p.Ile1291Phe
|
|
XM_017011106.2:c.3742A>T
|
XP_016866595.1:p.Ile1248Phe
|
|
XM_017011107.2:c.3721A>T
|
XP_016866596.1:p.Ile1241Phe
|
|
XR_002956289.1:n.4113A>T
|
|
|
NM_001363725.2:c.1570A>T
|
NP_001350654.1:p.Ile524Phe
|
|
NM_001371656.1:c.3949A>T
|
NP_001358585.1:p.Ile1317Phe
|
|
NM_001374820.1:c.3949A>T
|
NP_001361749.1:p.Ile1317Phe
|
|
NM_001374828.1:c.4069A>T
MANE Select
|
NP_001361757.1:p.Ile1357Phe
|
|
NM_017519.3:c.3910A>T
|
NP_059989.3:p.Ile1304Phe
|
|