ENST00000624552.4:c.14972G>C
|
ENSP00000485357.2:p.Gly4991Ala
|
|
ENST00000683500.2:c.15029G>C
MANE Select
|
ENSP00000508292.2:p.Gly5010Ala
|
|
ENST00000623487.1:n.3375G>C
|
|
|
ENST00000624552.3:c.14969G>C
|
ENSP00000485357.1:p.Gly4990Ala
|
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NM_001291815.1:c.15029G>C
|
NP_001278744.1:p.Gly5010Ala
|
|
XM_011518465.1:c.14906G>C
|
XP_011516767.1:p.Gly4969Ala
|
|
XM_011518466.1:c.14897G>C
|
XP_011516768.1:p.Gly4966Ala
|
|
XM_011518467.1:c.14852G>C
|
XP_011516769.1:p.Gly4951Ala
|
|
NM_001291815.2:c.15029G>C
MANE Select
|
NP_001278744.1:p.Gly5010Ala
|
|
XM_011518465.2:c.14906G>C
|
XP_011516767.1:p.Gly4969Ala
|
|
XM_011518466.2:c.14897G>C
|
XP_011516768.1:p.Gly4966Ala
|
|
XM_011518467.2:c.14852G>C
|
XP_011516769.1:p.Gly4951Ala
|
|
XM_017014585.1:c.11810G>C
|
XP_016870074.1:p.Gly3937Ala
|
|
XM_017014586.1:c.7607G>C
|
XP_016870075.1:p.Gly2536Ala
|
|
XR_001746957.1:n.92+139C>G
|
|
|
XR_001746958.1:n.92+139C>G
|
|
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