ENST00000624552.4:c.14884T=
|
ENSP00000485357.2:p.Ser4962=
|
|
ENST00000683500.2:c.14941T=
MANE Select
|
ENSP00000508292.2:p.Ser4981=
|
|
ENST00000623487.1:n.3287T=
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|
|
ENST00000624552.3:c.14881T=
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ENSP00000485357.1:p.Ser4961=
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|
NM_001291815.1:c.14941T=
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NP_001278744.1:p.Ser4981=
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|
XM_011518465.1:c.14818T=
|
XP_011516767.1:p.Ser4940=
|
|
XM_011518466.1:c.14809T=
|
XP_011516768.1:p.Ser4937=
|
|
XM_011518467.1:c.14764T=
|
XP_011516769.1:p.Ser4922=
|
|
NM_001291815.2:c.14941T=
MANE Select
|
NP_001278744.1:p.Ser4981=
|
|
XM_011518465.2:c.14818T=
|
XP_011516767.1:p.Ser4940=
|
|
XM_011518466.2:c.14809T=
|
XP_011516768.1:p.Ser4937=
|
|
XM_011518467.2:c.14764T=
|
XP_011516769.1:p.Ser4922=
|
|
XM_017014585.1:c.11722T=
|
XP_016870074.1:p.Ser3908=
|
|
XM_017014586.1:c.7519T=
|
XP_016870075.1:p.Ser2507=
|
|
XR_001746957.1:n.92+227A=
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|
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XR_001746958.1:n.92+227A=
|
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