ENST00000449291.7:c.1583T>C
MANE Select
|
ENSP00000401508.2:p.Leu528Pro
|
|
ENST00000340490.7:c.1668T>C
|
ENSP00000341136.3:p.Pro556=
|
|
ENST00000426292.7:c.1544T>C
|
ENSP00000390949.3:p.Leu515Pro
|
|
ENST00000435154.7:c.*292T>C
|
ENSP00000405670.3:n.*292T>C
|
|
ENST00000449291.6:c.1583T>C
|
ENSP00000401508.2:p.Leu528Pro
|
|
ENST00000460623.5:c.607T>C
|
|
|
ENST00000464332.5:n.1127T>C
|
|
|
ENST00000498076.5:n.362T>C
|
|
|
ENST00000529179.1:n.367T>C
|
|
|
NM_001286829.1:c.1544T>C
|
NP_001273758.1:p.Leu515Pro
|
|
NM_145201.5:c.1583T>C
|
NP_660202.3:p.Leu528Pro
|
|
XM_011517377.1:c.1320T>C
|
XP_011515679.1:p.Pro440=
|
|
NM_001363145.1:c.1502T>C
|
NP_001350074.1:p.Leu501Pro
|
|
NM_001363146.1:c.899T>C
|
NP_001350075.1:p.Leu300Pro
|
|
XM_017013975.2:c.1887T>C
|
XP_016869464.1:p.Pro629=
|
|
XM_017013976.2:c.1802T>C
|
XP_016869465.1:p.Leu601Pro
|
|
XM_017013977.2:c.1587T>C
|
XP_016869466.1:p.Pro529=
|
|
XM_017013978.2:c.1539T>C
|
XP_016869467.1:p.Pro513=
|
|
XM_017013979.2:c.984T>C
|
XP_016869468.1:p.Pro328=
|
|
XM_024447332.1:c.957T>C
|
XP_024303100.1:p.Pro319=
|
|
XM_024447333.1:c.903T>C
|
XP_024303101.1:p.Pro301=
|
|
NM_145201.6:c.1583T>C
MANE Select
|
NP_660202.3:p.Leu528Pro
|
|
NM_001286829.2:c.1544T>C
|
NP_001273758.1:p.Leu515Pro
|
|