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NM_000061.3:c.1102G>T
MANE Select
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NP_000052.1:p.Gly368Ter
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ENST00000308731.8:c.1102G>T
MANE Select
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ENSP00000308176.8:p.Gly368Ter
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NM_000061.2:c.1102G>T , LRG_128t1:c.1102G>T
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NP_000052.1:p.Gly368Ter
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NM_001287344.1:c.1204G>T
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NP_001274273.1:p.Gly402Ter
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NM_001287344.2:c.1204G>T
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NP_001274273.1:p.Gly402Ter
|
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NM_001287345.1:c.1038+64G>T
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NP_001274274.1:n.1038+64G>T
|
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NM_001287345.2:c.1038+64G>T
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NP_001274274.1:n.1038+64G>T
|
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ENST00000308731.7:c.1102G>T
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ENSP00000308176.7:p.Gly368Ter
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ENST00000372880.5:c.1038+64G>T
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ENSP00000361971.1:n.1038+64G>T
|
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ENST00000470329.1:n.52G>T
|
|
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ENST00000478995.2:n.1262G>T
|
|
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ENST00000488970.2:n.1260G>T
|
|
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ENST00000618050.4:c.1102G>T
|
ENSP00000479125.1:p.Gly368Ter
|
|
ENST00000621635.4:c.1204G>T
|
ENSP00000483570.1:p.Gly402Ter
|
|
ENST00000695614.1:c.1102G>T
|
ENSP00000512053.1:p.Gly368Ter
|
|
ENST00000695615.1:c.1102G>T
|
ENSP00000512054.1:p.Gly368Ter
|
|
ENST00000695616.1:c.*947G>T
|
ENSP00000512055.1:n.*947G>T
|
|
ENST00000695617.1:c.1099G>T
|
ENSP00000512056.1:p.Gly367Ter
|
|
ENST00000695618.1:c.*851G>T
|
ENSP00000512058.1:n.*851G>T
|
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ENST00000695619.1:c.*812G>T
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ENSP00000512059.1:n.*812G>T
|
|
ENST00000695620.1:c.*947G>T
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ENSP00000512060.1:n.*947G>T
|
|
ENST00000695621.1:c.1102G>T
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ENSP00000512061.1:p.Gly368Ter
|
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ENST00000695622.1:c.1039G>T
|
ENSP00000512062.1:p.Gly347Ter
|
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ENST00000695623.1:c.1096G>T
|
ENSP00000512063.1:p.Gly366Ter
|
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ENST00000695624.1:n.407G>T
|
|
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ENST00000695625.1:c.1102G>T
|
ENSP00000512064.1:p.Gly368Ter
|
|
ENST00000695626.1:c.115G>T
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ENSP00000512065.1:p.Gly39Ter
|
|
ENST00000695627.1:c.115G>T
|
ENSP00000512066.1:p.Gly39Ter
|
|
ENST00000695628.1:c.115G>T
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ENSP00000512067.1:p.Gly39Ter
|
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ENST00000695629.1:c.115G>T
|
ENSP00000512068.1:p.Gly39Ter
|
|
ENST00000695630.1:c.111G>T
|
|
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ENST00000695631.1:c.114G>T
|
|
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ENST00000695632.1:n.119G>T
|
|
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ENST00000703407.1:c.1038+64G>T
|
ENSP00000512057.1:n.1038+64G>T
|
