ENST00000373207.2:c.3068G>T
MANE Select
|
ENSP00000362303.1:p.Gly1023Val
|
|
ENST00000373207.1:c.3068G>T
|
ENSP00000362303.1:p.Gly1023Val
|
|
ENST00000373208.5:c.3077G>T
|
ENSP00000362304.1:p.Gly1026Val
|
|
NM_080722.3:c.3068G>T
|
NP_542453.2:p.Gly1023Val
|
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NM_139155.2:c.3077G>T
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NP_631894.2:p.Gly1026Val
|
|
XM_011539300.1:c.2567G>T
|
XP_011537602.1:p.Gly856Val
|
|
XM_011539301.1:c.2141G>T
|
XP_011537603.1:p.Gly714Val
|
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XM_011539302.1:c.2141G>T
|
XP_011537604.1:p.Gly714Val
|
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XM_011539309.1:c.1637G>T
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XP_011537611.1:p.Gly546Val
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|
NM_080722.4:c.3068G>T
MANE Select
|
NP_542453.2:p.Gly1023Val
|
|
NM_139155.3:c.3077G>T
|
NP_631894.2:p.Gly1026Val
|
|
XM_011539300.2:c.2567G>T
|
XP_011537602.1:p.Gly856Val
|
|
XM_011539301.2:c.2141G>T
|
XP_011537603.1:p.Gly714Val
|
|
XM_011539302.2:c.2141G>T
|
XP_011537604.1:p.Gly714Val
|
|