ENST00000297784.10:c.582G=
MANE Select
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ENSP00000297784.6:p.Trp194=
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|
ENST00000644967.1:c.144G=
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ENSP00000496159.1:p.Trp48=
|
|
ENST00000645053.1:c.144G=
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ENSP00000493838.1:p.Trp48=
|
|
ENST00000645208.2:c.582G=
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ENSP00000494684.1:p.Trp194=
|
|
ENST00000645773.1:c.456G=
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ENSP00000493698.1:p.Trp152=
|
|
ENST00000645787.1:n.622G=
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|
|
ENST00000646619.1:c.144G=
|
ENSP00000493726.1:p.Trp48=
|
|
ENST00000650689.1:n.880G=
|
|
|
ENST00000651183.1:c.144G=
|
ENSP00000498723.1:p.Trp48=
|
|
ENST00000297784.9:c.582G=
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ENSP00000297784.5:p.Trp194=
|
|
ENST00000340019.4:c.582G=
|
ENSP00000341433.3:p.Trp194=
|
|
NM_138691.2:c.582G=
|
NP_619636.2:p.Trp194=
|
|
XM_011518213.1:c.1170G=
|
XP_011516515.1:p.Trp390=
|
|
XM_017014256.1:c.585G=
|
XP_016869745.1:p.Trp195=
|
|
NM_138691.3:c.582G=
MANE Select
|
NP_619636.2:p.Trp194=
|
|