ENST00000438773.4:c.1429C>T
MANE Select
|
ENSP00000405060.3:p.Pro477Ser
|
|
ENST00000648948.2:c.1429C>T
|
ENSP00000498020.1:p.Pro477Ser
|
|
ENST00000389328.8:c.1723C>T
|
ENSP00000373979.4:p.Pro575Ser
|
|
ENST00000438773.2:c.1429C>T
|
ENSP00000405060.2:p.Pro477Ser
|
|
ENST00000520857.5:c.959C>T
|
|
|
NM_001160372.2:c.1429C>T
|
NP_001153844.1:p.Pro477Ser
|
|
NM_031466.6:c.1723C>T
|
NP_113654.4:p.Pro575Ser
|
|
XM_005251077.3:c.1429C>T
|
XP_005251134.1:p.Pro477Ser
|
|
XM_011517326.1:c.1696C>T
|
XP_011515628.1:p.Pro566Ser
|
|
XM_011517327.1:c.1723C>T
|
XP_011515629.1:p.Pro575Ser
|
|
XM_011517328.1:c.1723C>T
|
XP_011515630.1:p.Pro575Ser
|
|
XM_011517329.1:c.817C>T
|
XP_011515631.1:p.Pro273Ser
|
|
XR_928355.1:n.1738C>T
|
|
|
NM_001160372.3:c.1429C>T
|
NP_001153844.1:p.Pro477Ser
|
|
NM_001321646.1:c.1402C>T
|
NP_001308575.1:p.Pro468Ser
|
|
NM_031466.7:c.1723C>T
|
NP_113654.4:p.Pro575Ser
|
|
XM_011517326.2:c.1696C>T
|
XP_011515628.1:p.Pro566Ser
|
|
XM_011517328.2:c.1723C>T
|
XP_011515630.1:p.Pro575Ser
|
|
XM_017013893.1:c.1723C>T
|
XP_016869382.1:p.Pro575Ser
|
|
XM_017013894.2:c.49C>T
|
XP_016869383.1:p.Pro17Ser
|
|
XR_928355.2:n.1738C>T
|
|
|
NM_001160372.4:c.1429C>T
MANE Select
|
NP_001153844.1:p.Pro477Ser
|
|
NM_001321646.2:c.1402C>T
|
NP_001308575.1:p.Pro468Ser
|
|
NM_001374682.1:c.1450C>T
|
NP_001361611.1:p.Pro484Ser
|
|
NM_001374683.1:c.1429C>T
|
NP_001361612.1:p.Pro477Ser
|
|
NM_001374684.1:c.1351+10848C>T
|
NP_001361613.1:n.1351+10848C>T
|
|
NM_031466.8:c.1429C>T
|
NP_113654.5:p.Pro477Ser
|
|
NR_164662.1:n.1518C>T
|
|
|