ENST00000313777.9:c.1158del
MANE Select
|
ENSP00000313309.4:p.Leu387PhefsTer?
|
|
ENST00000313777.8:c.1158del
|
ENSP00000313309.4:p.Leu387PhefsTer?
|
|
ENST00000377092.8:c.*898del
|
ENSP00000366296.5:n.*898del
|
|
ENST00000525130.5:c.*812del
|
ENSP00000433492.1:n.*812del
|
|
ENST00000525370.5:c.*815del
|
ENSP00000431420.1:n.*815del
|
|
ENST00000528094.5:c.1050del
|
ENSP00000435177.1:p.Leu351PhefsTer?
|
|
ENST00000529634.2:c.314del
|
|
|
ENST00000533418.5:c.1008del
|
ENSP00000431731.1:p.Leu337PhefsTer?
|
|
NM_001171937.1:c.1050del
|
NP_001165408.1:p.Leu351PhefsTer?
|
|
NM_025129.4:c.1158del
|
NP_079405.2:p.Leu387PhefsTer?
|
|
NR_033269.1:n.1277del
|
|
|
XM_006723399.2:c.*144del
|
XP_006723462.1:n.*144del
|
|
XM_011527339.1:c.1161del
|
XP_011525641.1:p.Leu388PhefsTer?
|
|
XM_011527340.1:c.1011del
|
XP_011525642.1:p.Leu338PhefsTer?
|
|
XM_011527341.1:c.1011del
|
XP_011525643.1:p.Leu338PhefsTer?
|
|
XM_011527342.1:c.990del
|
XP_011525644.1:p.Leu331PhefsTer?
|
|
XM_011527343.1:c.*144del
|
XP_011525645.1:n.*144del
|
|
XM_011527344.1:c.963del
|
XP_011525646.1:p.Leu322PhefsTer?
|
|
XM_011527345.1:c.861del
|
XP_011525647.1:p.Leu288PhefsTer?
|
|
XM_011527346.1:c.861del
|
XP_011525648.1:p.Leu288PhefsTer?
|
|
XM_011527347.1:c.861del
|
XP_011525649.1:p.Leu288PhefsTer?
|
|
NM_001352262.1:c.1161del
|
NP_001339191.1:p.Leu388PhefsTer?
|
|
NM_001363663.1:c.1008del
|
NP_001350592.1:p.Leu337PhefsTer?
|
|
XM_006723399.3:c.*144del
|
XP_006723462.1:n.*144del
|
|
XM_011527341.2:c.1011del
|
XP_011525643.1:p.Leu338PhefsTer?
|
|
XM_011527342.2:c.990del
|
XP_011525644.1:p.Leu331PhefsTer?
|
|
XM_017027321.1:c.858del
|
XP_016882810.1:p.Leu287PhefsTer?
|
|
XM_017027322.2:c.*144del
|
XP_016882811.1:n.*144del
|
|
XM_024451729.1:c.990del
|
XP_024307497.1:p.Leu331PhefsTer?
|
|
XM_024451730.1:c.987del
|
XP_024307498.1:p.Leu330PhefsTer?
|
|
XR_001753764.1:n.1933del
|
|
|
XR_001753765.1:n.1233del
|
|
|
XR_002958363.1:n.2184del
|
|
|
XR_002958364.1:n.1930del
|
|
|
XR_002958365.1:n.1823del
|
|
|
NM_001171937.2:c.1050del
|
NP_001165408.1:p.Leu351PhefsTer?
|
|
NM_001352262.2:c.1161del
|
NP_001339191.1:p.Leu388PhefsTer?
|
|
NM_025129.5:c.1158del
MANE Select
|
NP_079405.2:p.Leu387PhefsTer?
|
|
NR_033269.2:n.1259del
|
|
|