ENST00000684169.1:c.273C=
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ENSP00000506849.1:p.Leu91=
|
|
ENST00000392386.8:c.273C=
MANE Select
|
ENSP00000376188.2:p.Leu91=
|
|
ENST00000392386.7:c.273C=
|
ENSP00000376188.2:p.Leu91=
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|
NM_004750.4:c.273C=
|
NP_004741.1:p.Leu91=
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|
XM_011528422.1:c.207C=
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XP_011526724.1:p.Leu69=
|
|
XM_011528423.1:c.273C=
|
XP_011526725.1:p.Leu91=
|
|
XM_011528424.1:c.207C=
|
XP_011526726.1:p.Leu69=
|
|
XM_011528422.2:c.207C=
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XP_011526724.1:p.Leu69=
|
|
XM_011528423.2:c.273C=
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XP_011526725.1:p.Leu91=
|
|
XM_011528424.3:c.207C=
|
XP_011526726.1:p.Leu69=
|
|
NM_004750.5:c.273C=
MANE Select
|
NP_004741.1:p.Leu91=
|
|