ENST00000303115.8:c.379+1G>A
MANE Select
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ENSP00000306157.3:n.379+1G>A
|
|
ENST00000303115.7:c.379+1G>A
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ENSP00000306157.3:n.379+1G>A
|
|
ENST00000506850.5:c.379+1G>A
|
ENSP00000421207.1:n.379+1G>A
|
|
ENST00000511031.1:n.514G>A
|
|
|
ENST00000511982.1:c.380G>A
|
ENSP00000425309.1:p.Gly127Asp
|
|
ENST00000514217.5:c.379+1G>A
|
ENSP00000427688.1:n.379+1G>A
|
|
NM_002185.3:c.379+1G>A
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NP_002176.2:n.379+1G>A
|
|
NR_120485.1:n.482+1G>A
|
|
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XM_005248299.2:c.379+1G>A
|
XP_005248356.1:n.379+1G>A
|
|
XM_005248300.1:c.379+1G>A
|
XP_005248357.1:n.379+1G>A
|
|
XM_011514037.1:c.379+1G>A
|
XP_011512339.1:n.379+1G>A
|
|
NM_002185.4:c.379+1G>A
|
NP_002176.2:n.379+1G>A
|
|
NR_120485.2:n.508+1G>A
|
|
|
XM_005248299.4:c.379+1G>A
|
XP_005248356.1:n.379+1G>A
|
|
NM_002185.5:c.379+1G>A
MANE Select
|
NP_002176.2:n.379+1G>A
|
|
NR_120485.3:n.466+1G>A
|
|
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