ENST00000527168.6:n.730A=
|
|
|
ENST00000529110.2:c.715A=
|
ENSP00000435349.2:p.Thr239=
|
|
ENST00000529957.6:n.689A=
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|
|
ENST00000683366.1:c.*363A=
|
ENSP00000507283.1:n.*363A=
|
|
ENST00000683887.1:c.679A=
|
ENSP00000506886.1:p.Thr227=
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|
ENST00000684100.1:n.625A=
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|
|
ENST00000684126.1:n.765A=
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|
|
ENST00000684688.1:n.1256A=
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|
|
ENST00000204679.9:c.631A=
MANE Select
|
ENSP00000204679.4:p.Thr211=
|
|
ENST00000204679.8:c.631A=
|
ENSP00000204679.4:p.Thr211=
|
|
ENST00000527076.1:n.1854A=
|
|
|
ENST00000527168.5:n.798A=
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|
|
ENST00000529957.5:n.730A=
|
|
|
NM_032520.4:c.631A=
|
NP_115909.1:p.Thr211=
|
|
XM_017023782.1:c.679A=
|
XP_016879271.1:p.Thr227=
|
|
XM_017023783.1:c.271A=
|
XP_016879272.1:p.Thr91=
|
|
NM_032520.5:c.631A=
MANE Select
|
NP_115909.1:p.Thr211=
|
|