ENST00000313468.10:c.379A=
MANE Select
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ENSP00000315774.5:p.Thr127=
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ENST00000313468.9:c.379A=
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ENSP00000315774.5:p.Thr127=
|
|
ENST00000524810.5:c.311A=
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|
|
ENST00000525419.5:c.325A=
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ENSP00000433521.1:p.Thr109=
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|
ENST00000526339.5:c.379A=
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ENSP00000436287.1:p.Thr127=
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ENST00000526446.5:c.*434A=
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ENSP00000433645.1:n.*434A=
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|
ENST00000526542.1:n.330A=
|
|
|
ENST00000528492.1:c.-60A=
|
ENSP00000432848.1:n.-60A=
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|
ENST00000531282.1:n.231A=
|
|
|
NM_002496.3:c.379A=
|
NP_002487.1:p.Thr127=
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|
XM_005274013.1:c.379A=
|
XP_005274070.1:p.Thr127=
|
|
XM_005274014.1:c.379A=
|
XP_005274071.1:p.Thr127=
|
|
XM_005274015.1:c.259A=
|
XP_005274072.1:p.Thr87=
|
|
XM_011545053.1:c.379A=
|
XP_011543355.1:p.Thr127=
|
|
NM_002496.4:c.379A=
MANE Select
|
NP_002487.1:p.Thr127=
|
|