ENST00000389048.8:c.3554T>C
MANE Select
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ENSP00000373700.3:p.Val1185Ala
|
|
ENST00000431873.6:c.781T>C
|
|
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ENST00000638605.1:n.431T>C
|
|
|
ENST00000642122.1:c.350T>C
|
ENSP00000493203.1:p.Val117Ala
|
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ENST00000389048.7:c.3554T>C
|
ENSP00000373700.3:p.Val1185Ala
|
|
ENST00000431873.5:c.434T>C
|
ENSP00000414027.2:p.Val145Ala
|
|
ENST00000618119.4:c.2423T>C
|
ENSP00000482733.1:p.Val808Ala
|
|
NM_004304.4:c.3554T>C
|
NP_004295.2:p.Val1185Ala
|
|
NM_001353765.1:c.350T>C
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NP_001340694.1:p.Val117Ala
|
|
XM_024452778.1:c.707T>C
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XP_024308546.1:p.Val236Ala
|
|
XM_024452779.1:c.350T>C
|
XP_024308547.1:p.Val117Ala
|
|
NM_004304.5:c.3554T>C
MANE Select
|
NP_004295.2:p.Val1185Ala
|
|
NM_001353765.2:c.350T>C
|
NP_001340694.1:p.Val117Ala
|
|