ENST00000502274.2:c.3374+193G=
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|
|
ENST00000515425.6:c.3478+193G=
MANE Select
|
ENSP00000423660.1:n.3478+193G=
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ENST00000675793.1:c.*2955G=
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ENSP00000502039.1:n.*2955G=
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|
ENST00000323829.9:c.*2866+193G=
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ENSP00000313025.5:n.*2866+193G=
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|
ENST00000504517.5:c.3008+193G=
|
ENSP00000421779.1:n.3008+193G=
|
|
ENST00000504690.5:c.3478+193G=
|
ENSP00000425627.1:n.3478+193G=
|
|
ENST00000510779.1:c.2528+193G=
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|
|
ENST00000512049.5:c.3457+193G=
|
ENSP00000421860.1:n.3457+193G=
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|
ENST00000515229.5:n.140+193G=
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|
|
ENST00000515425.5:c.3478+193G=
|
ENSP00000423660.1:n.3478+193G=
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|
NM_024577.3:c.3478+193G= , LRG_269t1:c.3478+193G=
|
NP_078853.2:n.3478+193G=
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|
NM_024577.4:c.3478+193G=
MANE Select
|
NP_078853.2:n.3478+193G=
|
|