ENST00000295754.10:c.1106G>T
MANE Select
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ENSP00000295754.5:p.Gly369Val
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ENST00000672866.1:n.2702G>T
|
|
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ENST00000295754.9:c.1106G>T
|
ENSP00000295754.5:p.Gly369Val
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ENST00000359013.4:c.1181G>T
|
ENSP00000351905.4:p.Gly394Val
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NM_001024847.2:c.1181G>T , LRG_779t1:c.1181G>T
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NP_001020018.1:p.Gly394Val
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NM_003242.5:c.1106G>T
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NP_003233.4:p.Gly369Val
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XM_011534043.1:c.1133G>T
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XP_011532345.1:p.Gly378Val
|
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XM_011534044.1:c.1058G>T
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XP_011532346.1:p.Gly353Val
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XM_011534045.1:c.1001G>T
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XP_011532347.1:p.Gly334Val
|
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XM_011534043.2:c.1133G>T
|
XP_011532345.1:p.Gly378Val
|
|
XM_011534045.3:c.1001G>T
|
XP_011532347.1:p.Gly334Val
|
|
XM_017007106.1:c.1001G>T
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XP_016862595.1:p.Gly334Val
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NM_003242.6:c.1106G>T
MANE Select
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NP_003233.4:p.Gly369Val
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