|
ENST00000647165.2:c.6396C>A
MANE Select
|
ENSP00000495481.1:p.Ala2132=
|
|
|
ENST00000205890.9:c.6396C>A
|
ENSP00000205890.5:p.Ala2132=
|
|
|
ENST00000615845.4:c.6396C>A
|
ENSP00000481642.1:p.Ala2132=
|
|
|
NM_016239.3:c.6396C>A
|
NP_057323.3:p.Ala2132=
|
|
|
XM_011523917.1:c.6336C>A
|
XP_011522219.1:p.Ala2112=
|
|
|
XM_011523918.1:c.6336C>A
|
XP_011522220.1:p.Ala2112=
|
|
|
XM_011523921.1:c.6390C>A
|
XP_011522223.1:p.Ala2130=
|
|
|
XR_934037.1:n.6995C>A
|
|
|
|
XR_934038.1:n.6995C>A
|
|
|
|
XM_011523918.2:c.6336C>A
|
XP_011522220.1:p.Ala2112=
|
|
|
XM_017024714.2:c.6336C>A
|
XP_016880203.1:p.Ala2112=
|
|
|
XM_017024715.2:c.6399C>A
|
XP_016880204.1:p.Ala2133=
|
|
|
XM_024450781.1:c.6213+1402C>A
|
XP_024306549.1:n.6213+1402C>A
|
|
|
NM_016239.4:c.6396C>A
MANE Select
|
NP_057323.3:p.Ala2132=
|
|
