ENST00000696154.2:n.1494C>T
|
|
|
ENST00000696154.1:c.*704C>T
|
ENSP00000512445.1:n.*704C>T
|
|
ENST00000696155.1:n.270C>T
|
|
|
ENST00000259089.9:c.1386C>T
MANE Select
|
ENSP00000259089.4:p.Pro462=
|
|
ENST00000645242.1:c.1173C>T
|
ENSP00000494690.1:p.Pro391=
|
|
ENST00000259089.8:c.1386C>T
|
ENSP00000259089.4:p.Pro462=
|
|
ENST00000526097.1:n.1326C>T
|
|
|
ENST00000529894.1:c.1173C>T
|
ENSP00000433663.1:p.Pro391=
|
|
NM_001715.2:c.1386C>T
|
NP_001706.2:p.Pro462=
|
|
XM_011543824.1:c.1464C>T
|
XP_011542126.1:p.Pro488=
|
|
XM_011543825.1:c.1464C>T
|
XP_011542127.1:p.Pro488=
|
|
XM_011543826.1:c.1464C>T
|
XP_011542128.1:p.Pro488=
|
|
XM_011543827.1:c.1251C>T
|
XP_011542129.1:p.Pro417=
|
|
NM_001330465.1:c.1173C>T
|
NP_001317394.1:p.Pro391=
|
|
XM_011543825.3:c.1464C>T
|
XP_011542127.1:p.Pro488=
|
|
NM_001715.3:c.1386C>T
MANE Select
|
NP_001706.2:p.Pro462=
|
|
NM_001330465.2:c.1173C>T
|
NP_001317394.1:p.Pro391=
|
|