ENST00000622290.5:c.3725C=
|
ENSP00000483331.2:p.Thr1242=
|
|
ENST00000205557.12:c.3725C=
MANE Select
|
ENSP00000205557.7:p.Thr1242=
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ENST00000640696.1:c.539C=
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ENSP00000492197.1:p.Thr180=
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ENST00000205557.11:c.3725C=
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ENSP00000205557.7:p.Thr1242=
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ENST00000456970.6:c.3350C=
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ENSP00000405002.2:n.3350C=
|
|
ENST00000622290.4:c.*934C=
|
ENSP00000483331.1:n.*934C=
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|
NM_001171.5:c.3725C=
|
NP_001162.4:p.Thr1242=
|
|
XM_011522479.1:c.3692C=
|
XP_011520781.1:p.Thr1231=
|
|
XM_011522480.1:c.3383C=
|
XP_011520782.1:p.Thr1128=
|
|
XM_011522481.1:c.3383C=
|
XP_011520783.1:p.Thr1128=
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|
XR_932836.1:n.3960C=
|
|
|
XR_932837.1:n.3761C=
|
|
|
XR_932838.1:n.3761C=
|
|
|
XR_933134.1:n.539-289G=
|
|
|
NM_001351800.1:c.3383C=
|
NP_001338729.1:p.Thr1128=
|
|
NR_147784.1:n.3387C=
|
|
|
XM_011522479.2:c.3692C=
|
XP_011520781.1:p.Thr1231=
|
|
XM_011522481.3:c.3383C=
|
XP_011520783.1:p.Thr1128=
|
|
XM_017023212.1:c.3557C=
|
XP_016878701.1:p.Thr1186=
|
|
XM_024450261.1:c.3761C=
|
XP_024306029.1:p.Thr1254=
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|
XR_932836.2:n.3906C=
|
|
|
XR_932837.3:n.3706C=
|
|
|
XR_932838.3:n.3706C=
|
|
|
NM_001171.6:c.3725C=
MANE Select
|
NP_001162.5:p.Thr1242=
|
|