ENST00000406757.3:c.6C>T
|
|
|
ENST00000684880.1:c.*405C>T
|
ENSP00000510280.1:n.*405C>T
|
|
ENST00000689310.1:c.769C>T
|
ENSP00000510438.1:p.Pro257Ser
|
|
ENST00000692084.1:c.11C>T
|
|
|
ENST00000370818.8:c.817C>T
MANE Select
|
ENSP00000359854.3:p.Pro273Ser
|
|
ENST00000394299.7:c.817C>T
|
ENSP00000377836.2:p.Pro273Ser
|
|
ENST00000666673.1:n.11C>T
|
|
|
ENST00000370818.7:c.817C>T
|
ENSP00000359854.3:p.Pro273Ser
|
|
ENST00000394299.6:c.817C>T
|
ENSP00000377836.2:p.Pro273Ser
|
|
ENST00000406757.2:c.6C>T
|
|
|
ENST00000631057.2:c.655C>T
|
ENSP00000486325.1:p.Pro219Ser
|
|
NM_001164617.1:c.817C>T
|
NP_001158089.1:p.Pro273Ser
|
|
NM_001164618.1:c.769C>T
|
NP_001158090.1:p.Pro257Ser
|
|
NM_001164619.1:c.655C>T
|
NP_001158091.1:p.Pro219Ser
|
|
NM_004484.3:c.817C>T , LRG_505t1:c.817C>T
|
NP_004475.1:p.Pro273Ser
|
|
XM_017029413.2:c.817C>T
|
XP_016884902.1:p.Pro273Ser
|
|
NM_001164617.2:c.817C>T
|
NP_001158089.1:p.Pro273Ser
|
|
NM_001164618.2:c.769C>T
|
NP_001158090.1:p.Pro257Ser
|
|
NM_001164619.2:c.655C>T
|
NP_001158091.1:p.Pro219Ser
|
|
NM_004484.4:c.817C>T
MANE Select
|
NP_004475.1:p.Pro273Ser
|
|