|
ENST00000349215.8:c.2909T>C
MANE Select
|
ENSP00000265967.5:p.Phe970Ser
|
|
|
ENST00000349215.7:c.2909T>C
|
ENSP00000265967.5:p.Phe970Ser
|
|
|
ENST00000352460.7:n.1228+1203T>C
|
|
|
|
ENST00000396253.7:c.2567T>C
|
ENSP00000379552.3:p.Phe856Ser
|
|
|
ENST00000438420.6:c.2567T>C
|
ENSP00000399590.2:p.Phe856Ser
|
|
|
ENST00000537258.1:c.230T>C
|
ENSP00000437437.1:p.Phe77Ser
|
|
|
ENST00000544218.5:c.467T>C
|
ENSP00000441781.1:p.Phe156Ser
|
|
|
ENST00000545561.1:n.970T>C
|
|
|
|
NM_007216.3:c.2567T>C
|
NP_009147.3:p.Phe856Ser
|
|
|
NM_181507.1:c.2909T>C , LRG_586t1:c.2909T>C
|
NP_852608.1:p.Phe970Ser
|
|
|
NM_181508.1:c.2567T>C
|
NP_852609.1:p.Phe856Ser
|
|
|
XM_011519862.1:c.2909T>C
|
XP_011518164.1:p.Phe970Ser
|
|
|
XM_011519863.1:c.2909T>C
|
XP_011518165.1:p.Phe970Ser
|
|
|
XM_011519864.1:c.2909T>C
|
XP_011518166.1:p.Phe970Ser
|
|
|
XM_011519865.1:c.2798T>C
|
XP_011518167.1:p.Phe933Ser
|
|
|
XM_011519866.1:c.2567T>C
|
XP_011518168.1:p.Phe856Ser
|
|
|
XM_011519867.1:c.2567T>C
|
XP_011518169.1:p.Phe856Ser
|
|
|
XM_011519868.1:c.2567T>C
|
XP_011518170.1:p.Phe856Ser
|
|
|
XM_011519869.1:c.2909T>C
|
XP_011518171.1:p.Phe970Ser
|
|
|
XM_011519868.3:c.2567T>C
|
XP_011518170.1:p.Phe856Ser
|
|
|
XM_017017149.1:c.2909T>C
|
XP_016872638.1:p.Phe970Ser
|
|
|
XM_017017150.1:c.2909T>C
|
XP_016872639.1:p.Phe970Ser
|
|
|
XM_017017151.2:c.2798T>C
|
XP_016872640.1:p.Phe933Ser
|
|
|
XM_017017152.1:c.2798T>C
|
XP_016872641.1:p.Phe933Ser
|
|
|
XM_017017153.2:c.2798T>C
|
XP_016872642.1:p.Phe933Ser
|
|
|
XM_017017154.1:c.2567T>C
|
XP_016872643.1:p.Phe856Ser
|
|
|
XR_001747750.1:n.3178T>C
|
|
|
|
XR_001747751.1:n.3178T>C
|
|
|
|
XR_001747752.1:n.2934T>C
|
|
|
|
XR_001747753.1:n.3051T>C
|
|
|
|
XR_001747754.2:n.2575T>C
|
|
|
|
XR_001747755.2:n.2497T>C
|
|
|
|
XR_001747756.2:n.2510T>C
|
|
|
|
NM_007216.4:c.2567T>C
|
NP_009147.3:p.Phe856Ser
|
|
|
NM_181507.2:c.2909T>C
MANE Select
|
NP_852608.1:p.Phe970Ser
|
|
