ENST00000642496.1:c.4047T>G
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ENST00000644397.2:c.5188T>G
MANE Select
|
ENSP00000495195.1:p.Trp1730Gly
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ENST00000373965.6:c.4999T>G
|
ENSP00000363076.3:p.Trp1667Gly
|
|
ENST00000414778.5:c.4996T>G
|
ENSP00000410304.2:p.Trp1666Gly
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ENST00000495484.5:c.1216T>G
|
ENSP00000480780.1:p.Trp406Gly
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ENST00000614895.4:c.5011T>G
|
ENSP00000478512.1:p.Trp1671Gly
|
|
ENST00000616114.4:c.4993T>G
|
ENSP00000483745.1:p.Trp1665Gly
|
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ENST00000618301.4:c.1348T>G
|
ENSP00000482780.1:p.Trp450Gly
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ENST00000621708.4:c.5014T>G
|
ENSP00000484454.1:p.Trp1672Gly
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NM_001142771.1:c.5014T>G
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NP_001136243.1:p.Trp1672Gly
|
|
NM_001142772.1:c.4999T>G
|
NP_001136244.1:p.Trp1667Gly
|
|
NM_001354420.1:c.4993T>G
|
NP_001341349.1:p.Trp1665Gly
|
|
NM_001354429.1:c.5122T>G
|
NP_001341358.1:p.Trp1708Gly
|
|
XR_001747192.2:n.11480T>G
|
|
|
XR_001747193.2:n.11471T>G
|
|
|
NM_001142771.2:c.5014T>G
|
NP_001136243.1:p.Trp1672Gly
|
|
NM_001142772.2:c.4999T>G
|
NP_001136244.1:p.Trp1667Gly
|
|
NM_001354420.2:c.4993T>G
|
NP_001341349.1:p.Trp1665Gly
|
|
NM_001354429.2:c.5122T>G
|
NP_001341358.1:p.Trp1708Gly
|
|
NM_001384140.1:c.5188T>G
MANE Select
|
NP_001371069.1:p.Trp1730Gly
|
|