ENST00000585361.6:c.*395G>A
|
ENSP00000466983.1:n.*395G>A
|
|
ENST00000588558.6:c.*533G>A
|
ENSP00000467624.1:n.*533G>A
|
|
ENST00000590253.3:c.439G>A
|
ENSP00000465111.2:p.Asp147Asn
|
|
ENST00000593115.2:c.*579G>A
|
ENSP00000466821.1:n.*579G>A
|
|
ENST00000696383.1:c.213G>A
|
ENSP00000512593.1:p.Met71Ile
|
|
ENST00000696384.1:c.*118G>A
|
ENSP00000512594.1:n.*118G>A
|
|
ENST00000696385.1:c.*276G>A
|
ENSP00000512595.1:n.*276G>A
|
|
ENST00000696386.1:c.241G>A
|
ENSP00000512596.1:p.Asp81Asn
|
|
ENST00000696387.1:c.*185G>A
|
ENSP00000512597.1:n.*185G>A
|
|
ENST00000696388.1:c.*404G>A
|
ENSP00000512598.1:n.*404G>A
|
|
ENST00000696389.1:c.*589G>A
|
ENSP00000512599.1:n.*589G>A
|
|
ENST00000696390.1:c.348G>A
|
ENSP00000512600.1:p.Met116Ile
|
|
ENST00000696391.1:c.*414G>A
|
ENSP00000512601.1:n.*414G>A
|
|
ENST00000696392.1:c.558G>A
|
ENSP00000512602.1:p.Met186Ile
|
|
ENST00000696393.1:c.558G>A
|
ENSP00000512603.1:p.Met186Ile
|
|
ENST00000696405.1:c.558G>A
|
ENSP00000512607.1:p.Met186Ile
|
|
ENST00000269097.9:c.558G>A
MANE Select
|
ENSP00000269097.3:p.Met186Ile
|
|
ENST00000269097.8:c.558G>A
|
ENSP00000269097.3:p.Met186Ile
|
|
ENST00000585361.5:c.*395G>A
|
ENSP00000466983.1:n.*395G>A
|
|
ENST00000588558.5:c.*533G>A
|
ENSP00000467624.1:n.*533G>A
|
|
ENST00000590253.2:c.60G>A
|
|
|
ENST00000590639.1:n.579G>A
|
|
|
ENST00000591696.1:c.450G>A
|
ENSP00000468677.1:p.Met150Ile
|
|
NM_138387.3:c.558G>A , LRG_182t1:c.558G>A
|
NP_612396.1:p.Met186Ile
|
|
NR_028581.1:n.988G>A
|
|
|
NR_028582.1:n.853G>A
|
|
|
XM_006722179.2:c.439G>A
|
XP_006722242.1:p.Asp147Asn
|
|
XM_011525473.1:c.213G>A
|
XP_011523775.1:p.Met71Ile
|
|
XM_011525474.1:c.213G>A
|
XP_011523776.1:p.Met71Ile
|
|
NM_001319945.1:c.439G>A
|
NP_001306874.1:p.Asp147Asn
|
|
XM_011525473.3:c.213G>A
|
XP_011523775.1:p.Met71Ile
|
|
XM_011525474.3:c.213G>A
|
XP_011523776.1:p.Met71Ile
|
|
XM_017025335.2:c.213G>A
|
XP_016880824.1:p.Met71Ile
|
|
NM_001319945.2:c.439G>A
|
NP_001306874.1:p.Asp147Asn
|
|
NR_028581.2:n.807G>A
|
|
|
NR_028582.2:n.672G>A
|
|
|
NM_001384165.1:c.213G>A
|
NP_001371094.1:p.Met71Ile
|
|
NM_001384166.1:c.213G>A
|
NP_001371095.1:p.Met71Ile
|
|
NM_001384167.1:c.213G>A
|
NP_001371096.1:p.Met71Ile
|
|
NM_001384168.1:c.213G>A
|
NP_001371097.1:p.Met71Ile
|
|
NM_138387.4:c.558G>A
MANE Select
|
NP_612396.1:p.Met186Ile
|
|