ENST00000493477.2:n.1415T=
|
|
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ENST00000682162.1:c.941T=
|
ENSP00000508203.1:n.941T=
|
|
ENST00000682567.1:n.989T=
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|
|
ENST00000683521.1:c.912T=
|
ENSP00000506864.1:p.Pro304=
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|
ENST00000684161.1:n.2127T=
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|
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ENST00000684483.1:c.*308T=
|
ENSP00000507894.1:n.*308T=
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|
ENST00000366560.4:c.912T=
MANE Select
|
ENSP00000355518.4:p.Pro304=
|
|
ENST00000366560.3:c.912T=
|
ENSP00000355518.3:p.Pro304=
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|
NM_000143.3:c.912T= , LRG_504t1:c.912T=
|
NP_000134.2:p.Pro304=
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|
XM_011544132.1:c.684T=
|
XP_011542434.1:p.Pro228=
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|
XM_011544132.2:c.684T=
|
XP_011542434.1:p.Pro228=
|
|
NM_000143.4:c.912T=
MANE Select
|
NP_000134.2:p.Pro304=
|
|