ENST00000367574.9:c.329+99A>C
|
ENSP00000356546.6:n.329+99A>C
|
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ENST00000537758.6:c.329+99A>C
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ENSP00000446401.3:n.329+99A>C
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ENST00000682661.1:n.488+99A>C
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|
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ENST00000683923.1:c.329+99A>C
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ENSP00000506737.1:n.329+99A>C
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ENST00000684722.1:n.511+99A>C
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ENST00000326194.11:c.329+99A>C
MANE Select
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ENSP00000322304.6:n.329+99A>C
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ENST00000485288.7:c.258+99A>C
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ENSP00000420445.3:n.258+99A>C
|
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ENST00000326194.10:c.329+99A>C
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ENSP00000322304.6:n.329+99A>C
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ENST00000355092.4:c.194+99A>C
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ENSP00000347207.4:n.194+99A>C
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ENST00000355961.8:c.329+99A>C
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ENSP00000348233.4:n.329+99A>C
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ENST00000359882.8:c.329+99A>C
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ENSP00000352946.4:n.329+99A>C
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ENST00000361988.7:c.329+99A>C
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ENSP00000354978.3:n.329+99A>C
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ENST00000367574.8:c.329+99A>C
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ENSP00000356546.5:n.329+99A>C
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ENST00000470275.2:c.258+99A>C
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ENSP00000418644.2:n.258+99A>C
|
|
ENST00000472520.5:c.137-306A>C
|
ENSP00000419858.1:n.137-306A>C
|
|
ENST00000485288.6:c.450+99A>C
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ENSP00000420445.2:n.450+99A>C
|
|
ENST00000491243.5:n.368+99A>C
|
|
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ENST00000528612.5:c.258+99A>C
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ENSP00000431224.1:n.258+99A>C
|
|
ENST00000537758.5:c.329+99A>C
|
ENSP00000446401.2:n.329+99A>C
|
|
NM_001282167.1:c.116+99A>C
|
NP_001269096.1:n.116+99A>C
|
|
NM_022825.3:c.329+99A>C
|
NP_073736.2:n.329+99A>C
|
|
NM_203473.2:c.329+99A>C
|
NP_982299.1:n.329+99A>C
|
|
NM_203474.1:c.329+99A>C
|
NP_982300.1:n.329+99A>C
|
|
NM_203475.2:c.329+99A>C
|
NP_982301.1:n.329+99A>C
|
|
XM_005272635.1:c.668+99A>C
|
XP_005272692.1:n.668+99A>C
|
|
XM_005272636.1:c.668+99A>C
|
XP_005272693.1:n.668+99A>C
|
|
XM_005272637.1:c.581+99A>C
|
XP_005272694.1:n.581+99A>C
|
|
XM_006724544.2:c.434+99A>C
|
XP_006724607.1:n.434+99A>C
|
|
XM_006724545.2:c.380+99A>C
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XP_006724608.1:n.380+99A>C
|
|
XM_006724546.2:c.329+99A>C
|
XP_006724609.1:n.329+99A>C
|
|
XM_006724547.1:c.116+99A>C
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XP_006724610.1:n.116+99A>C
|
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XM_011543948.1:c.116+99A>C
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XP_011542250.1:n.116+99A>C
|
|
XM_024452425.1:c.668+99A>C
|
XP_024308193.1:n.668+99A>C
|
|
NM_001282167.2:c.116+99A>C
|
NP_001269096.1:n.116+99A>C
|
|
NM_022825.4:c.329+99A>C
|
NP_073736.2:n.329+99A>C
|
|
NM_203473.3:c.329+99A>C
|
NP_982299.1:n.329+99A>C
|
|
NM_203475.3:c.329+99A>C
MANE Select
|
NP_982301.1:n.329+99A>C
|
|