ENST00000703783.1:n.269G>T
|
|
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ENST00000703785.1:n.350G>T
|
|
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ENST00000262464.9:c.3485G>T
MANE Select
|
ENSP00000262464.4:p.Cys1162Phe
|
|
ENST00000262464.8:c.3485G>T
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ENSP00000262464.4:p.Cys1162Phe
|
|
ENST00000507835.5:c.35G>T
|
ENSP00000426839.1:p.Cys12Phe
|
|
ENST00000508053.5:c.3485G>T
|
ENSP00000424571.1:p.Cys1162Phe
|
|
ENST00000508989.5:c.3386G>T
|
ENSP00000425596.1:p.Cys1129Phe
|
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ENST00000619499.4:c.3482G>T
|
ENSP00000482132.1:p.Cys1161Phe
|
|
NM_001999.3:c.3485G>T
|
NP_001990.2:p.Cys1162Phe
|
|
XM_017009228.2:c.3332G>T
|
XP_016864717.1:p.Cys1111Phe
|
|
NM_001999.4:c.3485G>T
MANE Select
|
NP_001990.2:p.Cys1162Phe
|
|