ENST00000696154.2:n.1502A=
|
|
|
ENST00000696154.1:c.*712A=
|
ENSP00000512445.1:n.*712A=
|
|
ENST00000696155.1:n.278A=
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|
|
ENST00000259089.9:c.1394A=
MANE Select
|
ENSP00000259089.4:p.Tyr465=
|
|
ENST00000645242.1:c.1181A=
|
ENSP00000494690.1:p.Tyr394=
|
|
ENST00000259089.8:c.1394A=
|
ENSP00000259089.4:p.Tyr465=
|
|
ENST00000526097.1:n.1334A=
|
|
|
ENST00000529894.1:c.1181A=
|
ENSP00000433663.1:p.Tyr394=
|
|
NM_001715.2:c.1394A=
|
NP_001706.2:p.Tyr465=
|
|
XM_011543824.1:c.1472A=
|
XP_011542126.1:p.Tyr491=
|
|
XM_011543825.1:c.1472A=
|
XP_011542127.1:p.Tyr491=
|
|
XM_011543826.1:c.1472A=
|
XP_011542128.1:p.Tyr491=
|
|
XM_011543827.1:c.1259A=
|
XP_011542129.1:p.Tyr420=
|
|
NM_001330465.1:c.1181A=
|
NP_001317394.1:p.Tyr394=
|
|
XM_011543825.3:c.1472A=
|
XP_011542127.1:p.Tyr491=
|
|
NM_001715.3:c.1394A=
MANE Select
|
NP_001706.2:p.Tyr465=
|
|
NM_001330465.2:c.1181A=
|
NP_001317394.1:p.Tyr394=
|
|