ENST00000326840.11:c.422G>T
MANE Select
|
ENSP00000321573.6:p.Arg141Ile
|
|
ENST00000326840.10:c.422G>T
|
ENSP00000321573.6:p.Arg141Ile
|
|
ENST00000326857.9:c.422G>T
|
ENSP00000321646.9:p.Arg141Ile
|
|
ENST00000449482.1:c.104G>T
|
ENSP00000396803.1:p.Arg35Ile
|
|
ENST00000469648.5:n.268+19171G>T
|
|
|
ENST00000486004.1:n.400G>T
|
|
|
NM_080927.3:c.422G>T
|
NP_563615.3:p.Arg141Ile
|
|
XM_011512419.1:c.205+19571G>T
|
XP_011510721.1:n.205+19571G>T
|
|
XM_011512419.2:c.205+19571G>T
|
XP_011510721.1:n.205+19571G>T
|
|
XM_024453347.1:c.104G>T
|
XP_024309115.1:p.Arg35Ile
|
|
XM_024453348.1:c.104G>T
|
XP_024309116.1:p.Arg35Ile
|
|
NM_080927.4:c.422G>T
MANE Select
|
NP_563615.3:p.Arg141Ile
|
|