ENST00000525346.6:c.965G>T
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ENSP00000435707.3:p.Gly322Val
|
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ENST00000526780.6:c.965G>T
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ENSP00000435668.2:p.Gly322Val
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ENST00000527316.6:c.791G>T
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ENSP00000435047.2:p.Gly264Val
|
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ENST00000682708.1:c.1016G>T
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ENSP00000506866.1:p.Gly339Val
|
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ENST00000683287.1:c.1001G>T
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ENSP00000507607.1:p.Gly334Val
|
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ENST00000683714.1:c.973G>T
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ENSP00000508207.1:p.Val325Phe
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ENST00000684396.1:n.1005G>T
|
|
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ENST00000685320.1:c.380G>T
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ENSP00000509319.1:p.Gly127Val
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ENST00000690257.1:c.869G>T
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ENSP00000510750.1:p.Gly290Val
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ENST00000355527.8:c.965G>T
MANE Select
|
ENSP00000347717.4:p.Gly322Val
|
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ENST00000355527.7:c.965G>T
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ENSP00000347717.3:p.Gly322Val
|
|
ENST00000407721.6:c.965G>T
|
ENSP00000384739.2:p.Gly322Val
|
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ENST00000525137.1:c.466G>T
|
ENSP00000435956.1:p.Val156Phe
|
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ENST00000533800.5:c.215G>T
|
ENSP00000435011.1:p.Gly72Val
|
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ENST00000534795.5:c.319+1974G>T
|
|
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NM_001163817.1:c.965G>T
|
NP_001157289.1:p.Gly322Val
|
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NM_001360.2:c.965G>T , LRG_340t1:c.965G>T
|
NP_001351.2:p.Gly322Val
|
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XM_011544777.1:c.1099G>T
|
XP_011543079.1:p.Val367Phe
|
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XM_011544777.2:c.1099G>T
|
XP_011543079.1:p.Val367Phe
|
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NM_001163817.2:c.965G>T
|
NP_001157289.1:p.Gly322Val
|
|
NM_001360.3:c.965G>T
MANE Select
|
NP_001351.2:p.Gly322Val
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