ENST00000233627.14:c.396A>T
MANE Select
|
ENSP00000233627.9:p.Pro132=
|
|
ENST00000233627.13:c.396A>T
|
ENSP00000233627.9:p.Pro132=
|
|
ENST00000313408.11:c.396A>T
|
ENSP00000364262.5:p.Pro132=
|
|
ENST00000414651.3:c.486A>T
|
ENSP00000406630.2:p.Pro162=
|
|
ENST00000436115.6:n.2351A>T
|
|
|
ENST00000534853.5:c.*190A>T
|
ENSP00000442822.1:n.*190A>T
|
|
ENST00000535382.1:n.648A>T
|
|
|
ENST00000538523.5:n.452A>T
|
|
|
ENST00000538662.5:n.423A>T
|
|
|
ENST00000538929.5:n.486A>T
|
|
|
ENST00000539480.5:c.396A>T
|
ENSP00000443273.1:p.Pro132=
|
|
ENST00000540530.5:n.387A>T
|
|
|
ENST00000543289.5:n.886A>T
|
|
|
ENST00000545446.5:n.687A>T
|
|
|
ENST00000546172.7:c.*392A>T
|
ENSP00000467094.1:n.*392A>T
|
|
ENST00000546283.5:c.396A>T
|
ENSP00000440348.1:p.Pro132=
|
|
ENST00000618074.4:c.396A>T
|
ENSP00000477895.1:p.Pro132=
|
|
ENST00000620479.4:c.396A>T
|
ENSP00000480984.1:p.Pro132=
|
|
ENST00000622587.4:n.392A>T
|
|
|
NM_024407.4:c.396A>T
|
NP_077718.3:p.Pro132=
|
|
XM_005259556.3:c.396A>T
|
XP_005259613.2:p.Pro132=
|
|
NM_001363602.1:c.396A>T
|
NP_001350531.1:p.Pro132=
|
|
XM_024451499.1:c.417A>T
|
XP_024307267.1:p.Pro139=
|
|
NM_024407.5:c.396A>T
MANE Select
|
NP_077718.3:p.Pro132=
|
|
NM_001363602.2:c.396A>T
|
NP_001350531.1:p.Pro132=
|
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