ENST00000370096.9:c.2629G>C
MANE Select
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ENSP00000359114.3:p.Gly877Arg
|
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ENST00000353414.8:c.2512G>C
|
ENSP00000302551.6:p.Gly838Arg
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ENST00000358392.6:c.2665G>C
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ENSP00000351163.2:p.Gly889Arg
|
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ENST00000370096.7:c.2629G>C
|
ENSP00000359114.3:p.Gly877Arg
|
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ENST00000512756.5:c.2281G>C
|
ENSP00000426533.1:p.Gly761Arg
|
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ENST00000635193.1:c.1963G>C
|
|
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NM_001190709.1:c.2512G>C
|
NP_001177638.1:p.Gly838Arg
|
|
NM_001854.3:c.2629G>C
|
NP_001845.3:p.Gly877Arg
|
|
NM_080629.2:c.2665G>C
|
NP_542196.2:p.Gly889Arg
|
|
NM_080630.3:c.2281G>C
|
NP_542197.3:p.Gly761Arg
|
|
XM_011540719.1:c.2629G>C
|
XP_011539021.1:p.Gly877Arg
|
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XM_011540720.1:c.862G>C
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XP_011539022.1:p.Gly288Arg
|
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XM_011540721.1:c.217G>C
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XP_011539023.1:p.Gly73Arg
|
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XR_946545.1:n.3043G>C
|
|
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NR_134980.1:n.2963G>C
|
|
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XM_017000334.1:c.2782G>C
|
XP_016855823.1:p.Gly928Arg
|
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XM_017000335.1:c.2776G>C
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XP_016855824.1:p.Gly926Arg
|
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XM_017000336.1:c.2782G>C
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XP_016855825.1:p.Gly928Arg
|
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XM_017000337.1:c.1180G>C
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XP_016855826.1:p.Gly394Arg
|
|
NM_001854.4:c.2629G>C
MANE Select
|
NP_001845.3:p.Gly877Arg
|
|
NM_080630.4:c.2281G>C
|
NP_542197.3:p.Gly761Arg
|
|
NR_134980.2:n.2989G>C
|
|
|
NM_001190709.2:c.2512G>C
|
NP_001177638.1:p.Gly838Arg
|
|
NM_080629.3:c.2665G>C
|
NP_542196.2:p.Gly889Arg
|
|