ENST00000262367.10:c.4560+29T>A
MANE Select
|
ENSP00000262367.5:n.4560+29T>A
|
|
ENST00000262367.9:c.4560+29T>A
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ENSP00000262367.5:n.4560+29T>A
|
|
ENST00000382070.7:c.4446+29T>A
|
ENSP00000371502.3:n.4446+29T>A
|
|
ENST00000570939.2:c.3195+29T>A
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ENSP00000461002.2:n.3195+29T>A
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ENST00000571763.5:n.350+29T>A
|
|
|
ENST00000574740.1:n.410T>A
|
|
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ENST00000576720.1:n.3383+29T>A
|
|
|
NM_001079846.1:c.4446+29T>A
|
NP_001073315.1:n.4446+29T>A
|
|
NM_004380.2:c.4560+29T>A
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NP_004371.2:n.4560+29T>A
|
|
XM_005255124.3:c.4515+29T>A
|
XP_005255181.1:n.4515+29T>A
|
|
XM_005255125.3:c.4143+29T>A
|
XP_005255182.1:n.4143+29T>A
|
|
XM_006720848.2:c.4299+29T>A
|
XP_006720911.1:n.4299+29T>A
|
|
XM_011522380.1:c.4506+29T>A
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XP_011520682.1:n.4506+29T>A
|
|
XM_011522381.1:c.3807+29T>A
|
XP_011520683.1:n.3807+29T>A
|
|
XM_005255124.4:c.4515+29T>A
|
XP_005255181.1:n.4515+29T>A
|
|
XM_005255125.4:c.4143+29T>A
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XP_005255182.1:n.4143+29T>A
|
|
XM_006720848.3:c.4299+29T>A
|
XP_006720911.1:n.4299+29T>A
|
|
XM_011522381.2:c.3807+29T>A
|
XP_011520683.1:n.3807+29T>A
|
|
XM_017022944.1:c.4554+29T>A
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XP_016878433.1:n.4554+29T>A
|
|
NM_004380.3:c.4560+29T>A
MANE Select
|
NP_004371.2:n.4560+29T>A
|
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