ENST00000684241.1:n.3574G>T
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ENST00000262186.10:c.2741G>T
MANE Select
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ENSP00000262186.5:p.Gly914Val
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ENST00000330883.9:c.1721G>T
|
ENSP00000328531.4:p.Gly574Val
|
|
ENST00000262186.9:c.2741G>T
|
ENSP00000262186.5:p.Gly914Val
|
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ENST00000330883.8:c.1721G>T
|
ENSP00000328531.4:p.Gly574Val
|
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NM_000238.3:c.2741G>T , LRG_288t1:c.2741G>T
|
NP_000229.1:p.Gly914Val
|
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NM_172057.2:c.1721G>T , LRG_288t3:c.1721G>T
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NP_742054.1:p.Gly574Val
|
|
XM_011516185.1:c.2441G>T
|
XP_011514487.1:p.Gly814Val
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XM_011516186.1:c.2693-139G>T
|
XP_011514488.1:n.2693-139G>T
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XM_011516185.2:c.2441G>T
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XP_011514487.1:p.Gly814Val
|
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XM_011516186.3:c.2693-139G>T
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XP_011514488.1:n.2693-139G>T
|
|
XM_017012195.1:c.2591G>T
|
XP_016867684.1:p.Gly864Val
|
|
XM_017012196.1:c.2564G>T
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XP_016867685.1:p.Gly855Val
|
|
NM_000238.4:c.2741G>T
MANE Select
|
NP_000229.1:p.Gly914Val
|
|
NM_172057.3:c.1721G>T
|
NP_742054.1:p.Gly574Val
|
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