ENST00000673913.2:c.1504-102A=
|
ENSP00000501161.2:n.1504-102A=
|
|
ENST00000710286.1:c.1861-102A=
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ENSP00000518176.1:n.1861-102A=
|
|
ENST00000673903.1:c.1129-102A=
|
ENSP00000501257.1:n.1129-102A=
|
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ENST00000673913.1:c.244-102A=
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ENSP00000501161.1:n.244-102A=
|
|
ENST00000302118.5:c.1504-102A=
MANE Select
|
ENSP00000303208.5:n.1504-102A=
|
|
ENST00000490692.1:n.2227+737A=
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|
|
NM_174936.3:c.1504-102A= , LRG_275t1:c.1504-102A=
|
NP_777596.2:n.1504-102A=
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|
NR_110451.1:n.1111-102A=
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|
|
XM_011541193.1:c.625-102A=
|
XP_011539495.1:n.625-102A=
|
|
NM_174936.4:c.1504-102A=
MANE Select
|
NP_777596.2:n.1504-102A=
|
|
NR_110451.2:n.1111-102A=
|
|
|