ENST00000350026.11:c.3911T=
|
ENSP00000055163.8:p.Ile1304=
|
|
ENST00000414678.8:c.3980T=
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ENSP00000412835.3:p.Ile1327=
|
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ENST00000637015.2:c.4199T=
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ENSP00000489729.2:p.Ile1400=
|
|
ENST00000346085.10:c.3950T=
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ENSP00000344546.5:p.Ile1317=
|
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ENST00000350026.10:c.3662T=
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ENSP00000055163.7:p.Ile1221=
|
|
ENST00000414678.7:c.2228T=
|
ENSP00000412835.2:p.Ile743=
|
|
ENST00000635849.1:c.1391T=
|
ENSP00000490948.1:p.Ile464=
|
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ENST00000635957.1:c.1022T=
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ENSP00000490385.1:p.Ile341=
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|
ENST00000636930.2:c.4070T=
MANE Select
|
ENSP00000490491.2:p.Ile1357=
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ENST00000636940.1:n.2067T=
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|
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ENST00000637015.1:c.1438T=
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ENST00000637568.1:c.1352T=
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ENST00000637741.1:n.736T=
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|
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ENST00000637810.1:c.1412T=
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ENSP00000489636.1:p.Ile471=
|
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ENST00000637904.1:c.1571T=
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ENSP00000490550.1:p.Ile524=
|
|
ENST00000647938.1:c.3701T=
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ENSP00000498155.1:p.Ile1234=
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ENST00000346085.9:c.3701T=
|
ENSP00000344546.4:p.Ile1234=
|
|
ENST00000350026.9:c.3662T=
|
ENSP00000055163.7:p.Ile1221=
|
|
ENST00000414678.6:c.2228T=
|
ENSP00000412835.2:p.Ile743=
|
|
NM_017519.2:c.3662T=
|
NP_059989.2:p.Ile1221=
|
|
NM_020732.3:c.3701T=
|
NP_065783.3:p.Ile1234=
|
|
XM_005267069.3:c.3821T=
|
XP_005267126.2:p.Ile1274=
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|
XM_011535984.1:c.2900T=
|
XP_011534286.1:p.Ile967=
|
|
XM_011535985.1:c.2720T=
|
XP_011534287.1:p.Ile907=
|
|
XM_011535986.1:c.2480T=
|
XP_011534288.1:p.Ile827=
|
|
XM_011535987.1:c.2099T=
|
XP_011534289.1:p.Ile700=
|
|
XM_011535988.1:c.962T=
|
XP_011534290.1:p.Ile321=
|
|
NM_001346813.1:c.3821T=
|
NP_001333742.1:p.Ile1274=
|
|
NM_001363725.1:c.1571T=
|
NP_001350654.1:p.Ile524=
|
|
XM_011535984.2:c.4031T=
|
XP_011534286.2:p.Ile1344=
|
|
XM_011535988.3:c.962T=
|
XP_011534290.1:p.Ile321=
|
|
XM_017011103.2:c.3932T=
|
XP_016866592.1:p.Ile1311=
|
|
XM_017011104.1:c.3902T=
|
XP_016866593.1:p.Ile1301=
|
|
XM_017011105.2:c.3872T=
|
XP_016866594.1:p.Ile1291=
|
|
XM_017011106.2:c.3743T=
|
XP_016866595.1:p.Ile1248=
|
|
XM_017011107.2:c.3722T=
|
XP_016866596.1:p.Ile1241=
|
|
XR_002956289.1:n.4114T=
|
|
|
NM_001363725.2:c.1571T=
|
NP_001350654.1:p.Ile524=
|
|
NM_001371656.1:c.3950T=
|
NP_001358585.1:p.Ile1317=
|
|
NM_001374820.1:c.3950T=
|
NP_001361749.1:p.Ile1317=
|
|
NM_001374828.1:c.4070T=
MANE Select
|
NP_001361757.1:p.Ile1357=
|
|
NM_017519.3:c.3911T=
|
NP_059989.3:p.Ile1304=
|
|