ENST00000682153.1:c.*458A>C
|
ENSP00000507923.1:n.*458A>C
|
|
ENST00000682358.1:n.11434A>C
|
|
|
ENST00000683334.1:c.*7046A>C
|
ENSP00000507369.1:n.*7046A>C
|
|
ENST00000357162.7:c.11289A>C
MANE Select
|
ENSP00000349685.2:p.Gly3763=
|
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ENST00000358544.7:c.11364A>C
MANE Plus Clinical
|
ENSP00000351346.2:p.Gly3788=
|
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ENST00000357162.6:c.11289A>C
|
ENSP00000349685.2:p.Gly3763=
|
|
ENST00000358544.6:c.11364A>C
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ENSP00000351346.2:p.Gly3788=
|
|
ENST00000493587.1:n.306A>C
|
|
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NM_017890.4:c.11364A>C , LRG_351t1:c.11364A>C
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NP_060360.3:p.Gly3788=
|
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NM_152564.4:c.11289A>C , LRG_351t2:c.11289A>C
|
NP_689777.3:p.Gly3763=
|
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XM_005250800.2:c.11364A>C
|
XP_005250857.1:p.Gly3788=
|
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XM_005250801.3:c.11364A>C
|
XP_005250858.1:p.Gly3788=
|
|
XM_011516848.1:c.11361A>C
|
XP_011515150.1:p.Gly3787=
|
|
XM_011516849.1:c.11286A>C
|
XP_011515151.1:p.Gly3762=
|
|
XM_011516850.1:c.10986A>C
|
XP_011515152.1:p.Gly3662=
|
|
XM_011516851.1:c.8250A>C
|
XP_011515153.1:p.Gly2750=
|
|
XM_011516852.1:c.8250A>C
|
XP_011515154.1:p.Gly2750=
|
|
XM_011516854.1:c.7143A>C
|
XP_011515156.1:p.Gly2381=
|
|
XM_005250800.3:c.11364A>C
|
XP_005250857.1:p.Gly3788=
|
|
XM_005250801.5:c.11364A>C
|
XP_005250858.1:p.Gly3788=
|
|
XM_011516848.2:c.11361A>C
|
XP_011515150.1:p.Gly3787=
|
|
XM_011516849.2:c.11286A>C
|
XP_011515151.1:p.Gly3762=
|
|
XM_011516850.2:c.10986A>C
|
XP_011515152.1:p.Gly3662=
|
|
XM_011516851.2:c.8250A>C
|
XP_011515153.1:p.Gly2750=
|
|
XM_011516852.2:c.8250A>C
|
XP_011515154.1:p.Gly2750=
|
|
XM_011516854.2:c.7143A>C
|
XP_011515156.1:p.Gly2381=
|
|
XM_017013109.1:c.11169A>C
|
XP_016868598.1:p.Gly3723=
|
|
XM_017013111.1:c.8250A>C
|
XP_016868600.1:p.Gly2750=
|
|
XM_017013112.1:c.6921A>C
|
XP_016868601.1:p.Gly2307=
|
|
XM_024447074.1:c.10149A>C
|
XP_024302842.1:p.Gly3383=
|
|
NM_017890.5:c.11364A>C
MANE Plus Clinical
|
NP_060360.3:p.Gly3788=
|
|
NM_152564.5:c.11289A>C
MANE Select
|
NP_689777.3:p.Gly3763=
|
|