|
NM_001130823.3:c.4636C>T
MANE Select
|
NP_001124295.1:p.Pro1546Ser
|
|
ENST00000359526.9:c.4636C>T
MANE Select
|
ENSP00000352516.3:p.Pro1546Ser
|
|
NM_001130823.1:c.4636C>T , LRG_362t1:c.4636C>T
|
NP_001124295.1:p.Pro1546Ser
|
|
NM_001130823.2:c.4636C>T
|
NP_001124295.1:p.Pro1546Ser
|
|
NM_001318730.1:c.4597C>T
|
NP_001305659.1:p.Pro1533Ser
|
|
NM_001318730.2:c.4597C>T
|
NP_001305659.1:p.Pro1533Ser
|
|
NM_001318731.1:c.4273C>T
|
NP_001305660.1:p.Pro1425Ser
|
|
NM_001318731.2:c.4273C>T
|
NP_001305660.1:p.Pro1425Ser
|
|
NM_001379.2:c.4588C>T
|
NP_001370.1:p.Pro1530Ser
|
|
NM_001379.3:c.4588C>T
|
NP_001370.1:p.Pro1530Ser
|
|
NM_001379.4:c.4588C>T
|
NP_001370.1:p.Pro1530Ser
|
|
ENST00000340748.8:c.4588C>T
|
ENSP00000345739.3:p.Pro1530Ser
|
|
ENST00000359526.8:c.4636C>T
|
ENSP00000352516.3:p.Pro1546Ser
|
|
ENST00000540357.5:c.3580C>T
|
ENSP00000440457.2:p.Pro1194Ser
|
|
ENST00000586588.5:n.2509C>T
|
|
|
ENST00000586667.2:n.2671C>T
|
|
|
ENST00000588913.5:c.915C>T
|
|
|
ENST00000589351.6:n.3822C>T
|
|
|
ENST00000592705.5:c.*4326C>T
|
ENSP00000466657.1:n.*4326C>T
|
|
ENST00000676604.1:n.4248C>T
|
|
|
ENST00000676610.1:c.4588C>T
|
ENSP00000504236.1:p.Pro1530Ser
|
|
ENST00000676820.1:n.5482C>T
|
|
|
ENST00000676868.1:n.5272C>T
|
|
|
ENST00000677013.1:c.*4278C>T
|
ENSP00000503135.1:n.*4278C>T
|
|
ENST00000677038.1:n.1184C>T
|
|
|
ENST00000677250.1:c.*3708C>T
|
ENSP00000502894.1:n.*3708C>T
|
|
ENST00000677616.1:c.*858C>T
|
ENSP00000503055.1:n.*858C>T
|
|
ENST00000677634.1:c.*1191C>T
|
ENSP00000504246.1:n.*1191C>T
|
|
ENST00000677685.1:c.*3813C>T
|
ENSP00000503407.1:n.*3813C>T
|
|
ENST00000677783.1:n.5896C>T
|
|
|
ENST00000677946.1:c.4588C>T
|
ENSP00000504202.1:p.Pro1530Ser
|
|
ENST00000678024.1:n.5569C>T
|
|
|
ENST00000678107.1:n.1631C>T
|
|
|
ENST00000678239.1:n.1489C>T
|
|
|
ENST00000678647.1:n.2730C>T
|
|
|
ENST00000678694.1:n.3909C>T
|
|
|
ENST00000678804.1:c.4597C>T
|
ENSP00000503853.1:p.Pro1533Ser
|
|
ENST00000678851.1:n.630C>T
|
|
|
ENST00000678957.1:n.2300C>T
|
|
|
ENST00000679100.1:n.2775C>T
|
|
|
ENST00000679103.1:c.4588C>T
|
ENSP00000503151.1:p.Pro1530Ser
|
|
ENST00000679313.1:c.4597C>T
|
ENSP00000504512.1:p.Pro1533Ser
|
|
XM_011527772.1:c.4645C>T
|
XP_011526074.1:p.Pro1549Ser
|
|
XM_011527773.1:c.4597C>T
|
XP_011526075.1:p.Pro1533Ser
|
|
XM_011527774.1:c.4234C>T
|
XP_011526076.1:p.Pro1412Ser
|