ENST00000326840.11:c.417C=
MANE Select
|
ENSP00000321573.6:p.Val139=
|
|
ENST00000326840.10:c.417C=
|
ENSP00000321573.6:p.Val139=
|
|
ENST00000326857.9:c.417C=
|
ENSP00000321646.9:p.Val139=
|
|
ENST00000449482.1:c.99C=
|
ENSP00000396803.1:p.Val33=
|
|
ENST00000469648.5:n.268+19166C=
|
|
|
ENST00000486004.1:n.395C=
|
|
|
NM_080927.3:c.417C=
|
NP_563615.3:p.Val139=
|
|
XM_011512419.1:c.205+19566C=
|
XP_011510721.1:n.205+19566C=
|
|
XM_011512419.2:c.205+19566C=
|
XP_011510721.1:n.205+19566C=
|
|
XM_024453347.1:c.99C=
|
XP_024309115.1:p.Val33=
|
|
XM_024453348.1:c.99C=
|
XP_024309116.1:p.Val33=
|
|
NM_080927.4:c.417C=
MANE Select
|
NP_563615.3:p.Val139=
|
|