ENST00000534624.6:c.1144G>C
MANE Select
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ENSP00000432083.1:p.Gly382Arg
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ENST00000227378.7:c.1144G>C
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ENSP00000227378.3:p.Gly382Arg
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ENST00000453788.6:c.1144G>C
|
ENSP00000404372.2:p.Gly382Arg
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ENST00000524552.5:c.-84G>C
|
ENSP00000435908.1:n.-84G>C
|
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ENST00000526110.5:c.1087G>C
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ENSP00000433584.1:p.Gly363Arg
|
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ENST00000526862.1:n.422G>C
|
|
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ENST00000527983.5:n.1504G>C
|
|
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ENST00000532091.1:n.891G>C
|
|
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ENST00000532636.5:c.1144G>C
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ENSP00000437125.1:p.Gly382Arg
|
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ENST00000533238.5:n.381-135G>C
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|
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ENST00000533540.5:c.706G>C
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ENSP00000437189.1:p.Gly236Arg
|
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ENST00000534319.5:c.436G>C
|
ENSP00000433316.1:p.Gly146Arg
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ENST00000534624.5:c.1144G>C
|
ENSP00000432083.1:p.Gly382Arg
|
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NM_006597.5:c.1144G>C
|
NP_006588.1:p.Gly382Arg
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NM_153201.3:c.1144G>C
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NP_694881.1:p.Gly382Arg
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XM_011542798.1:c.1144G>C
|
XP_011541100.1:p.Gly382Arg
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NM_006597.6:c.1144G>C
MANE Select
|
NP_006588.1:p.Gly382Arg
|
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NM_153201.4:c.1144G>C
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NP_694881.1:p.Gly382Arg
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