ENST00000378302.7:c.1160T>G
MANE Select
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ENSP00000367552.2:p.Val387Gly
|
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ENST00000258646.3:c.1160T>G
|
ENSP00000258646.3:p.Val387Gly
|
|
ENST00000378302.6:c.1160T>G
|
ENSP00000367552.2:p.Val387Gly
|
|
NM_018191.3:c.1160T>G
|
NP_060661.3:p.Val387Gly
|
|
XM_005266441.2:c.1160T>G
|
XP_005266498.1:p.Val387Gly
|
|
XM_011535133.1:c.1160T>G
|
XP_011533435.1:p.Val387Gly
|
|
XM_011535134.1:c.1160T>G
|
XP_011533436.1:p.Val387Gly
|
|
XM_011535135.1:c.773T>G
|
XP_011533437.1:p.Val258Gly
|
|
XR_941613.1:n.3733T>G
|
|
|
NM_001352500.1:c.1160T>G
|
NP_001339429.1:p.Val387Gly
|
|
NM_001352501.1:c.1160T>G
|
NP_001339430.1:p.Val387Gly
|
|
NM_001352502.1:c.1160T>G
|
NP_001339431.1:p.Val387Gly
|
|
NM_001352503.1:c.1160T>G
|
NP_001339432.1:p.Val387Gly
|
|
NM_001352504.1:c.1160T>G
|
NP_001339433.1:p.Val387Gly
|
|
NM_001352506.1:c.581T>G
|
NP_001339435.1:p.Val194Gly
|
|
NR_148015.1:n.1579T>G
|
|
|
NR_148016.1:n.1535T>G
|
|
|
XM_011535135.2:c.773T>G
|
XP_011533437.1:p.Val258Gly
|
|
XR_001749596.1:n.3082T>G
|
|
|
NM_018191.4:c.1160T>G
MANE Select
|
NP_060661.3:p.Val387Gly
|
|
NM_001352500.2:c.1160T>G
|
NP_001339429.1:p.Val387Gly
|
|
NM_001352501.2:c.1160T>G
|
NP_001339430.1:p.Val387Gly
|
|
NM_001352502.2:c.1160T>G
|
NP_001339431.1:p.Val387Gly
|
|
NM_001352503.2:c.1160T>G
|
NP_001339432.1:p.Val387Gly
|
|
NM_001352506.2:c.581T>G
|
NP_001339435.1:p.Val194Gly
|
|
NR_148015.2:n.1554T>G
|
|
|
NR_148016.2:n.1510T>G
|
|
|
NM_001352504.2:c.1160T>G
|
NP_001339433.1:p.Val387Gly
|
|