ENST00000325385.12:c.1660-9640T>A
MANE Select
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ENSP00000315569.7:n.1660-9640T>A
|
|
ENST00000273009.10:c.1581+27038T>A
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ENSP00000273009.6:n.1581+27038T>A
|
|
ENST00000325385.11:c.1660-9640T>A
|
ENSP00000315569.7:n.1660-9640T>A
|
|
ENST00000390005.9:c.1660-9640T>A
|
ENSP00000374655.5:n.1660-9640T>A
|
|
ENST00000409307.5:c.1660-9640T>A
|
ENSP00000386799.1:n.1660-9640T>A
|
|
ENST00000424049.1:c.565-9640T>A
|
ENSP00000415419.1:n.565-9640T>A
|
|
ENST00000433430.5:c.2814-9640T>A
|
ENSP00000391175.1:n.2814-9640T>A
|
|
ENST00000445090.5:c.*886-9640T>A
|
ENSP00000388999.1:n.*886-9640T>A
|
|
ENST00000498319.2:n.242-9640T>A
|
|
|
NM_001257281.1:c.1581+27038T>A
|
NP_001244210.1:n.1581+27038T>A
|
|
NM_152383.4:c.1660-9640T>A , LRG_534t1:c.1660-9640T>A
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NP_689596.4:n.1660-9640T>A
|
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NR_046476.1:n.1936-9640T>A
|
|
|
NR_046477.1:n.1912-9640T>A
|
|
|
NM_001257281.2:c.1581+27038T>A
|
NP_001244210.1:n.1581+27038T>A
|
|
NM_152383.5:c.1660-9640T>A
MANE Select
|
NP_689596.4:n.1660-9640T>A
|
|
NR_046476.2:n.1806-9640T>A
|
|
|
NR_046477.2:n.1782-9640T>A
|
|
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