ENST00000642496.1:c.3952A>G
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|
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ENST00000644397.2:c.5093A>G
MANE Select
|
ENSP00000495195.1:p.Gln1698Arg
|
|
ENST00000373965.6:c.4904A>G
|
ENSP00000363076.3:p.Gln1635Arg
|
|
ENST00000414778.5:c.4901A>G
|
ENSP00000410304.2:p.Gln1634Arg
|
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ENST00000495484.5:c.1121A>G
|
ENSP00000480780.1:p.Gln374Arg
|
|
ENST00000614895.4:c.4916A>G
|
ENSP00000478512.1:p.Gln1639Arg
|
|
ENST00000616114.4:c.4898A>G
|
ENSP00000483745.1:p.Gln1633Arg
|
|
ENST00000618301.4:c.1253A>G
|
ENSP00000482780.1:p.Gln418Arg
|
|
ENST00000621708.4:c.4919A>G
|
ENSP00000484454.1:p.Gln1640Arg
|
|
NM_001142771.1:c.4919A>G
|
NP_001136243.1:p.Gln1640Arg
|
|
NM_001142772.1:c.4904A>G
|
NP_001136244.1:p.Gln1635Arg
|
|
NM_001354420.1:c.4898A>G
|
NP_001341349.1:p.Gln1633Arg
|
|
NM_001354429.1:c.5027A>G
|
NP_001341358.1:p.Gln1676Arg
|
|
XR_001747192.2:n.11385A>G
|
|
|
XR_001747193.2:n.11376A>G
|
|
|
NM_001142771.2:c.4919A>G
|
NP_001136243.1:p.Gln1640Arg
|
|
NM_001142772.2:c.4904A>G
|
NP_001136244.1:p.Gln1635Arg
|
|
NM_001354420.2:c.4898A>G
|
NP_001341349.1:p.Gln1633Arg
|
|
NM_001354429.2:c.5027A>G
|
NP_001341358.1:p.Gln1676Arg
|
|
NM_001384140.1:c.5093A>G
MANE Select
|
NP_001371069.1:p.Gln1698Arg
|
|