NM_016213.5:c.1576-180G>C
MANE Select
|
NP_057297.2:n.1576-180G>C
|
ENST00000261884.8:c.1576-180G>C
MANE Select
|
ENSP00000261884.3:n.1576-180G>C
|
NM_001321924.1:c.886-180G>C
|
NP_001308853.1:n.886-180G>C
|
NM_001321924.2:c.886-180G>C
|
NP_001308853.1:n.886-180G>C
|
NM_016213.4:c.1576-180G>C
|
NP_057297.2:n.1576-180G>C
|
NR_135855.1:n.1509-180G>C
|
|
NR_135855.2:n.1477-180G>C
|
|
ENST00000261884.7:c.1576-180G>C
|
ENSP00000261884.3:n.1576-180G>C
|
ENST00000558162.1:c.134-180G>C
|
|
ENST00000559777.1:n.82+86G>C
|
|
ENST00000560475.1:c.112-180G>C
|
|
XM_005254789.1:c.886-180G>C
|
XP_005254846.1:n.886-180G>C
|
XR_243130.1:n.1507-180G>C
|
|
XR_932366.1:n.410C>G
|
|
XR_932367.1:n.196C>G
|
|
XR_932367.2:n.301C>G
|
|