ENST00000585361.6:c.*629C=
|
ENSP00000466983.1:n.*629C=
|
|
ENST00000588558.6:c.*767C=
|
ENSP00000467624.1:n.*767C=
|
|
ENST00000590253.3:c.*85C=
|
ENSP00000465111.2:n.*85C=
|
|
ENST00000593115.2:c.*813C=
|
ENSP00000466821.1:n.*813C=
|
|
ENST00000696383.1:c.447C=
|
ENSP00000512593.1:p.Ala149=
|
|
ENST00000696384.1:c.*352C=
|
ENSP00000512594.1:n.*352C=
|
|
ENST00000696385.1:c.*510C=
|
ENSP00000512595.1:n.*510C=
|
|
ENST00000696386.1:c.*85C=
|
ENSP00000512596.1:n.*85C=
|
|
ENST00000696387.1:c.*419C=
|
ENSP00000512597.1:n.*419C=
|
|
ENST00000696388.1:c.*638C=
|
ENSP00000512598.1:n.*638C=
|
|
ENST00000696389.1:c.*823C=
|
ENSP00000512599.1:n.*823C=
|
|
ENST00000696390.1:c.582C=
|
ENSP00000512600.1:p.Ala194=
|
|
ENST00000696391.1:c.*648C=
|
ENSP00000512601.1:n.*648C=
|
|
ENST00000696392.1:c.792C=
|
ENSP00000512602.1:p.Ala264=
|
|
ENST00000696393.1:c.792C=
|
ENSP00000512603.1:p.Ala264=
|
|
ENST00000696405.1:c.677+343C=
|
ENSP00000512607.1:n.677+343C=
|
|
ENST00000269097.9:c.792C=
MANE Select
|
ENSP00000269097.3:p.Ala264=
|
|
ENST00000269097.8:c.792C=
|
ENSP00000269097.3:p.Ala264=
|
|
ENST00000585361.5:c.*629C=
|
ENSP00000466983.1:n.*629C=
|
|
ENST00000588558.5:c.*767C=
|
ENSP00000467624.1:n.*767C=
|
|
ENST00000590253.2:c.294C=
|
|
|
ENST00000590639.1:n.813C=
|
|
|
ENST00000591696.1:c.684C=
|
ENSP00000468677.1:p.Ala228=
|
|
NM_138387.3:c.792C= , LRG_182t1:c.792C=
|
NP_612396.1:p.Ala264=
|
|
NR_028581.1:n.1222C=
|
|
|
NR_028582.1:n.1087C=
|
|
|
XM_011525473.1:c.447C=
|
XP_011523775.1:p.Ala149=
|
|
XM_011525474.1:c.447C=
|
XP_011523776.1:p.Ala149=
|
|
NM_001319945.1:c.*85C=
|
NP_001306874.1:n.*85C=
|
|
XM_011525473.3:c.447C=
|
XP_011523775.1:p.Ala149=
|
|
XM_011525474.3:c.447C=
|
XP_011523776.1:p.Ala149=
|
|
XM_017025335.2:c.447C=
|
XP_016880824.1:p.Ala149=
|
|
NM_001319945.2:c.*85C=
|
NP_001306874.1:n.*85C=
|
|
NR_028581.2:n.1041C=
|
|
|
NR_028582.2:n.906C=
|
|
|
NM_001384165.1:c.447C=
|
NP_001371094.1:p.Ala149=
|
|
NM_001384166.1:c.447C=
|
NP_001371095.1:p.Ala149=
|
|
NM_001384167.1:c.447C=
|
NP_001371096.1:p.Ala149=
|
|
NM_001384168.1:c.447C=
|
NP_001371097.1:p.Ala149=
|
|
NM_138387.4:c.792C=
MANE Select
|
NP_612396.1:p.Ala264=
|
|