ENST00000642496.1:c.3948G>A
|
|
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ENST00000644397.2:c.5089G>A
MANE Select
|
ENSP00000495195.1:p.Glu1697Lys
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|
ENST00000373965.6:c.4900G>A
|
ENSP00000363076.3:p.Glu1634Lys
|
|
ENST00000414778.5:c.4897G>A
|
ENSP00000410304.2:p.Glu1633Lys
|
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ENST00000495484.5:c.1117G>A
|
ENSP00000480780.1:p.Glu373Lys
|
|
ENST00000614895.4:c.4912G>A
|
ENSP00000478512.1:p.Glu1638Lys
|
|
ENST00000616114.4:c.4894G>A
|
ENSP00000483745.1:p.Glu1632Lys
|
|
ENST00000618301.4:c.1249G>A
|
ENSP00000482780.1:p.Glu417Lys
|
|
ENST00000621708.4:c.4915G>A
|
ENSP00000484454.1:p.Glu1639Lys
|
|
NM_001142771.1:c.4915G>A
|
NP_001136243.1:p.Glu1639Lys
|
|
NM_001142772.1:c.4900G>A
|
NP_001136244.1:p.Glu1634Lys
|
|
NM_001354420.1:c.4894G>A
|
NP_001341349.1:p.Glu1632Lys
|
|
NM_001354429.1:c.5023G>A
|
NP_001341358.1:p.Glu1675Lys
|
|
XR_001747192.2:n.11381G>A
|
|
|
XR_001747193.2:n.11372G>A
|
|
|
NM_001142771.2:c.4915G>A
|
NP_001136243.1:p.Glu1639Lys
|
|
NM_001142772.2:c.4900G>A
|
NP_001136244.1:p.Glu1634Lys
|
|
NM_001354420.2:c.4894G>A
|
NP_001341349.1:p.Glu1632Lys
|
|
NM_001354429.2:c.5023G>A
|
NP_001341358.1:p.Glu1675Lys
|
|
NM_001384140.1:c.5089G>A
MANE Select
|
NP_001371069.1:p.Glu1697Lys
|
|