ENST00000298139.7:c.3504C>G
MANE Select
|
ENSP00000298139.5:p.Ala1168=
|
|
ENST00000650667.1:c.*3118C>G
|
ENSP00000498593.1:n.*3118C>G
|
|
ENST00000298139.5:c.3504C>G
|
ENSP00000298139.5:p.Ala1168=
|
|
ENST00000521620.5:n.2137C>G
|
|
|
NM_000553.4:c.3504C>G , LRG_524t1:c.3504C>G
|
NP_000544.2:p.Ala1168=
|
|
XM_011544639.1:c.3423C>G
|
XP_011542941.1:p.Ala1141=
|
|
XM_011544640.1:c.1905C>G
|
XP_011542942.1:p.Ala635=
|
|
XR_949470.1:n.3777C>G
|
|
|
XR_949471.1:n.3777C>G
|
|
|
XR_949472.1:n.3777C>G
|
|
|
XR_949643.1:n.614+1100G>C
|
|
|
NM_000553.5:c.3504C>G
|
NP_000544.2:p.Ala1168=
|
|
XM_011544639.3:c.3423C>G
|
XP_011542941.1:p.Ala1141=
|
|
XM_024447265.1:c.3294C>G
|
XP_024303033.1:p.Ala1098=
|
|
XR_949470.3:n.3805C>G
|
|
|
XR_949471.3:n.3805C>G
|
|
|
XR_949472.3:n.3805C>G
|
|
|
NM_000553.6:c.3504C>G
MANE Select
|
NP_000544.2:p.Ala1168=
|
|