ENST00000399503.4:c.633+768A>G
MANE Select
|
ENSP00000382423.3:n.633+768A>G
|
|
ENST00000399503.3:c.633+768A>G
|
ENSP00000382423.3:n.633+768A>G
|
|
NM_005921.1:c.633+768A>G
|
NP_005912.1:n.633+768A>G
|
|
XM_005248519.3:c.255+768A>G
|
XP_005248576.2:n.255+768A>G
|
|
XM_011543406.1:c.378+768A>G
|
XP_011541708.1:n.378+768A>G
|
|
XM_011543407.1:c.633+768A>G
|
XP_011541709.1:n.633+768A>G
|
|
XM_011543408.1:c.633+768A>G
|
XP_011541710.1:n.633+768A>G
|
|
XM_017009484.1:c.222+768A>G
|
XP_016864973.1:n.222+768A>G
|
|
XM_017009485.1:c.144+768A>G
|
XP_016864974.1:n.144+768A>G
|
|
XR_001742068.2:n.664+768A>G
|
|
|
NM_005921.2:c.633+768A>G
MANE Select
|
NP_005912.1:n.633+768A>G
|
|