|
ENST00000269217.11:c.3517G=
MANE Plus Clinical
|
ENSP00000269217.5:p.Asp1173=
|
|
|
ENST00000313654.14:c.8344G=
MANE Select
|
ENSP00000324532.8:p.Asp2782=
|
|
|
ENST00000649721.1:c.4939G=
|
ENSP00000497885.1:p.Asp1647=
|
|
|
ENST00000269217.10:c.3517G=
|
ENSP00000269217.5:p.Asp1173=
|
|
|
ENST00000313654.13:c.8344G=
|
ENSP00000324532.8:p.Asp2782=
|
|
|
ENST00000399516.7:c.8176G=
|
ENSP00000382432.2:p.Asp2726=
|
|
|
ENST00000586751.5:c.3122G=
|
|
|
|
ENST00000587184.5:c.3349G=
|
ENSP00000466557.1:p.Asp1117=
|
|
|
ENST00000588164.2:c.49G=
|
ENSP00000467473.2:p.Asp17=
|
|
|
ENST00000588770.5:n.2922G=
|
|
|
|
NM_000227.4:c.3517G=
|
NP_000218.3:p.Asp1173=
|
|
|
NM_001127717.2:c.8176G=
|
NP_001121189.2:p.Asp2726=
|
|
|
NM_001127718.2:c.3349G=
|
NP_001121190.2:p.Asp1117=
|
|
|
NM_198129.2:c.8344G=
|
NP_937762.2:p.Asp2782=
|
|
|
XM_011525978.1:c.8371G=
|
XP_011524280.1:p.Asp2791=
|
|
|
XM_011525979.1:c.8362G=
|
XP_011524281.1:p.Asp2788=
|
|
|
XM_011525980.1:c.8353G=
|
XP_011524282.1:p.Asp2785=
|
|
|
XM_011525981.1:c.8239G=
|
XP_011524283.1:p.Asp2747=
|
|
|
XM_011525982.1:c.8074G=
|
XP_011524284.1:p.Asp2692=
|
|
|
XM_011525978.2:c.8371G=
|
XP_011524280.1:p.Asp2791=
|
|
|
XM_011525979.2:c.8362G=
|
XP_011524281.1:p.Asp2788=
|
|
|
XM_011525980.2:c.8353G=
|
XP_011524282.1:p.Asp2785=
|
|
|
XM_011525981.2:c.8239G=
|
XP_011524283.1:p.Asp2747=
|
|
|
XM_011525982.2:c.8074G=
|
XP_011524284.1:p.Asp2692=
|
|
|
XM_017025743.1:c.6223G=
|
XP_016881232.1:p.Asp2075=
|
|
|
XM_017025744.1:c.3913G=
|
XP_016881233.1:p.Asp1305=
|
|
|
XR_001753199.1:n.8612G=
|
|
|
|
NM_000227.5:c.3517G=
|
NP_000218.3:p.Asp1173=
|
|
|
NM_001127717.3:c.8176G=
|
NP_001121189.2:p.Asp2726=
|
|
|
NM_001127718.3:c.3349G=
|
NP_001121190.2:p.Asp1117=
|
|
|
NM_198129.3:c.8344G=
|
NP_937762.2:p.Asp2782=
|
|
|
NM_000227.6:c.3517G=
MANE Plus Clinical
|
NP_000218.3:p.Asp1173=
|
|
|
NM_001127717.4:c.8176G=
|
NP_001121189.2:p.Asp2726=
|
|
|
NM_001127718.4:c.3349G=
|
NP_001121190.2:p.Asp1117=
|
|
|
NM_198129.4:c.8344G=
MANE Select
|
NP_937762.2:p.Asp2782=
|
|
